Trials that use: Multiple imputation / missing data
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5,024 results
- A Cross-Over Study to Evaluate Lung Function Response After Treatment With Umeclidinium (UMEC) 62.5 Micrograms (mcg), Vilanterol (VI) 25 mcg, and Umeclidinium/Vilanterol (UMEC/VI) 62.5/25 mcg Once-Daily in Subjects With Chronic Obstructive Pulmonary Disease (COPD): Complete Statistical AnalysisIndependent statistical analysis of A Cross-Over Study to Evaluate Lung Function Response After Treatment With Umeclidinium (UMEC) 62.5 Micrograms (mcg), Vilanterol (VI) 25 mcg, and Umeclidinium/Vilanterol (UMEC/VI) 62.5/25 mcg Once-Daily in Subjects…
- A Crossover Study on the Blinding Effect of a New Pragmatic Placebo Needle: Complete Statistical AnalysisIndependent statistical analysis of A Crossover Study on the Blinding Effect of a New Pragmatic Placebo Needle: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on…
- A Crossover Study to Assess the Effects of Vorinostat (MK0683, SAHA) in Patients With Advanced Cancer (0683-070)(COMPLETED): Complete Statistical AnalysisIndependent statistical analysis of A Crossover Study to Assess the Effects of Vorinostat (MK0683, SAHA) in Patients With Advanced Cancer (0683-070)(COMPLETED): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration,…
- A Delphi Survey for Key Stakeholders to Identify Priority Self-management Outcomes for Chronic Kidney Disease: Complete Statistical AnalysisIndependent statistical analysis of A Delphi Survey for Key Stakeholders to Identify Priority Self-management Outcomes for Chronic Kidney Disease: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- A Digital Intervention to Prevent the Initiation of Opioid Misuse in Adolescents in School-based Health Centers: Complete Statistical AnalysisIndependent statistical analysis of A Digital Intervention to Prevent the Initiation of Opioid Misuse in Adolescents in School-based Health Centers: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and…
- A Dispensing Clinical Trial of a Study Test Silicone Hydrogel Lens Against Control Lens Over 1 Week: Complete Statistical AnalysisIndependent statistical analysis of A Dispensing Clinical Trial of a Study Test Silicone Hydrogel Lens Against Control Lens Over 1 Week: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration,…
- A Dose Escalation Safety Study of Locally-Delivered Gemcitabine in Pancreatic Cancer: Complete Statistical AnalysisIndependent statistical analysis of A Dose Escalation Safety Study of Locally-Delivered Gemcitabine in Pancreatic Cancer: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results…
- A Dose Escalation Study of MLN7243 (TAK-243) in Adult Participants With Advanced Solid Tumors: Complete Statistical AnalysisIndependent statistical analysis of A Dose Escalation Study of MLN7243 (TAK-243) in Adult Participants With Advanced Solid Tumors: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- A Dose Escalation Study of PF-06650808 in Patients With Advanced Solid Tumors: Complete Statistical AnalysisIndependent statistical analysis of A Dose Escalation Study of PF-06650808 in Patients With Advanced Solid Tumors: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov…
- A Dose Escalation/Expansion Study of Oral OP-1250 in Subjects With Advanced and/or Metastatic HR+, HER2- Breast Cancer: Complete Statistical AnalysisIndependent statistical analysis of A Dose Escalation/Expansion Study of Oral OP-1250 in Subjects With Advanced and/or Metastatic HR+, HER2- Breast Cancer: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration,…
- A Dose Linearity Study of the Labopharm Formulation of Tramadol HCl/Contramid®, 100 mg, 200 mg and 300 mg After A Single Oral Administration In Fasting Condition, In Healthy Human Volunteers: Complete Statistical AnalysisIndependent statistical analysis of A Dose Linearity Study of the Labopharm Formulation of Tramadol HCl/Contramid®, 100 mg, 200 mg and 300 mg After A Single Oral Administration In Fasting Condition, In Healthy…
- A Dose Proportionality Study of Quinine Sulfate Capsules Under Fasting Conditions: Complete Statistical AnalysisIndependent statistical analysis of A Dose Proportionality Study of Quinine Sulfate Capsules Under Fasting Conditions: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results…
- A Dose Ranging Effect of Preoperative Diphenhydramine on Postoperative Quality of Recovery After Ambulatory Surgery: Complete Statistical AnalysisIndependent statistical analysis of A Dose Ranging Effect of Preoperative Diphenhydramine on Postoperative Quality of Recovery After Ambulatory Surgery: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- A Dose Ranging Placebo-Controlled Double-Blind Study to Evaluate the Safety and Efficacy of Tezepelumab in Atopic Dermatitis: Complete Statistical AnalysisIndependent statistical analysis of A Dose Ranging Placebo-Controlled Double-Blind Study to Evaluate the Safety and Efficacy of Tezepelumab in Atopic Dermatitis: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration,…
- A Dose Ranging Study Of PF-00868554 In Combination With PEGASYS And COPEGUS In Patients With Chronic Hepatitis C Genotype 1 Infection: Complete Statistical AnalysisIndependent statistical analysis of A Dose Ranging Study Of PF-00868554 In Combination With PEGASYS And COPEGUS In Patients With Chronic Hepatitis C Genotype 1 Infection: primary endpoint results, effect estimate with confidence…
- A Dose-Escalating Study of Obinutuzumab in Patients With B-lymphocyte Antigen (CD20+) Malignant Disease (GAUGUIN): Complete Statistical AnalysisIndependent statistical analysis of A Dose-Escalating Study of Obinutuzumab in Patients With B-lymphocyte Antigen (CD20+) Malignant Disease (GAUGUIN): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- A Dose-Escalation Study Evaluating the Combination of Trastuzumab Emtansine (T-DM1) With Neratinib in Women With Metastatic HER2-Positive Breast Cancer: Complete Statistical AnalysisIndependent statistical analysis of A Dose-Escalation Study Evaluating the Combination of Trastuzumab Emtansine (T-DM1) With Neratinib in Women With Metastatic HER2-Positive Breast Cancer: primary endpoint results, effect estimate with confidence interval, sample-size…
- A Dose-Escalation to Rash Study of Tarceva (Erlotinib) Plus Gemcitabine in Patients With Metastatic Pancreatic Cancer: Complete Statistical AnalysisIndependent statistical analysis of A Dose-Escalation to Rash Study of Tarceva (Erlotinib) Plus Gemcitabine in Patients With Metastatic Pancreatic Cancer: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and…
- A Dose-finding and Confirmatory Trial of OPC-6535 in Patients With Active Crohn’s Disease: Complete Statistical AnalysisIndependent statistical analysis of A Dose-finding and Confirmatory Trial of OPC-6535 in Patients With Active Crohn's Disease: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on…
- A Dose-finding Study of OPC-6535 in Patients With Active Crohn’s Disease: Complete Statistical AnalysisIndependent statistical analysis of A Dose-finding Study of OPC-6535 in Patients With Active Crohn's Disease: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results…
- A Dose-ranging Pediatric Study of an Adjuvanted Pandemic Influenza Vaccine: Complete Statistical AnalysisIndependent statistical analysis of A Dose-ranging Pediatric Study of an Adjuvanted Pandemic Influenza Vaccine: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT04669691).
- A Dose-ranging Study of DRM01 in Subjects With Acne Vulgaris: Complete Statistical AnalysisIndependent statistical analysis of A Dose-ranging Study of DRM01 in Subjects With Acne Vulgaris: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT02431052).
- A Dose-response Trial Using rFSH FE 999049 in Women Undergoing IVF/ICSI Treatment: Complete Statistical AnalysisIndependent statistical analysis of A Dose-response Trial Using rFSH FE 999049 in Women Undergoing IVF/ICSI Treatment: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov…
- A Double Blind Clinical Trial of DCS for Food Anxiety: Complete Statistical AnalysisIndependent statistical analysis of A Double Blind Clinical Trial of DCS for Food Anxiety: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT01996644).
- A Double-Blind Placebo-Control Dose Escalating Study to Evaluate the Safety and Immunogenicity of dmLT by Oral, Sublingual and Intradermal Vaccination in Adults Residing in an Endemic Area: Complete Statistical AnalysisIndependent statistical analysis of A Double-Blind Placebo-Control Dose Escalating Study to Evaluate the Safety and Immunogenicity of dmLT by Oral, Sublingual and Intradermal Vaccination in Adults Residing in an Endemic Area: primary…
- A Double-Blind Single-Ascending Dose (SAD) and Multiple-Ascending Dose (MAD) Study to Investigate the Safety, Tolerability, and Pharmacokinetics of RO7049389 in Healthy Chinese Participants: Complete Statistical AnalysisIndependent statistical analysis of A Double-Blind Single-Ascending Dose (SAD) and Multiple-Ascending Dose (MAD) Study to Investigate the Safety, Tolerability, and Pharmacokinetics of RO7049389 in Healthy Chinese Participants: primary endpoint results, effect estimate…
- A Double-blind, Placebo-controlled, Crossover Study to Assess the Effect of Aclidinium Bromide 400 μg Bid on COPD Symptoms and Sleep Quality After 3 Weeks of Treatment in Patients With Stable Moderate-to-severe Chronic Obstructive Pulmonary Disease (COPD): Complete Statistical AnalysisIndependent statistical analysis of A Double-blind, Placebo-controlled, Crossover Study to Assess the Effect of Aclidinium Bromide 400 μg Bid on COPD Symptoms and Sleep Quality After 3 Weeks of Treatment in Patients…
- A Drug Interaction Study to Assess the Effect of LY2603618 on the Metabolic Pathway of Desipramine: Complete Statistical AnalysisIndependent statistical analysis of A Drug Interaction Study to Assess the Effect of LY2603618 on the Metabolic Pathway of Desipramine: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and…
- A Drug-Drug Interaction (DDI) Study of Orforglipron With Carbamazepine in Healthy Participants: Complete Statistical AnalysisIndependent statistical analysis of A Drug-Drug Interaction (DDI) Study of Orforglipron With Carbamazepine in Healthy Participants: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov…
- A Drug-Drug Interaction Study Between Fenofibric Acid and Efavirenz: Complete Statistical AnalysisIndependent statistical analysis of A Drug-Drug Interaction Study Between Fenofibric Acid and Efavirenz: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT01472380).
- A Drug-Drug Interaction Study to Assess the Pharmacokinetics of DC-806 When Orally Administered Alone, When Coadministered With Itraconazole, and When Coadministered With Carbamazepine in Healthy Adult Participants: Complete Statistical AnalysisIndependent statistical analysis of A Drug-Drug Interaction Study to Assess the Pharmacokinetics of DC-806 When Orally Administered Alone, When Coadministered With Itraconazole, and When Coadministered With Carbamazepine in Healthy Adult Participants: primary…
- A Drug-drug Interaction Study With Risdiplam Multiple Dose and Midazolam in Healthy Participants: Complete Statistical AnalysisIndependent statistical analysis of A Drug-drug Interaction Study With Risdiplam Multiple Dose and Midazolam in Healthy Participants: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on…
- A Duloxetine Dosing Strategy Study in Korean Patients With Major Depressive Disorder: Complete Statistical AnalysisIndependent statistical analysis of A Duloxetine Dosing Strategy Study in Korean Patients With Major Depressive Disorder: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov…
- A Efficacy, Safety, and Tolerability Study of Canagliflozin in Patients With Type 2 Diabetes Mellitus With Inadequate Glycemic Control on Metformin Alone or in Combination With a Sulphonylurea: Complete Statistical AnalysisIndependent statistical analysis of A Efficacy, Safety, and Tolerability Study of Canagliflozin in Patients With Type 2 Diabetes Mellitus With Inadequate Glycemic Control on Metformin Alone or in Combination With a Sulphonylurea:…
- A Feasibility Study of a Modular Video Augmentation System for Image-Guided Skull Base Surgery: Complete Statistical AnalysisIndependent statistical analysis of A Feasibility Study of a Modular Video Augmentation System for Image-Guided Skull Base Surgery: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- A Feasibility Study of the Cordis Neurovascular Self Expanding Stent System in Intracranial Arteries: Complete Statistical AnalysisIndependent statistical analysis of A Feasibility Study of the Cordis Neurovascular Self Expanding Stent System in Intracranial Arteries: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- A First Human Study of a Ferroportin Antibody: Complete Statistical AnalysisIndependent statistical analysis of A First Human Study of a Ferroportin Antibody: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT01330953).
- A First in Human Study to Evaluate Safety, Tolerability, and Pharmacology of PF-06826647 in Healthy Subjects and Subjects With Plaque Psoriasis: Complete Statistical AnalysisIndependent statistical analysis of A First in Human Study to Evaluate Safety, Tolerability, and Pharmacology of PF-06826647 in Healthy Subjects and Subjects With Plaque Psoriasis: primary endpoint results, effect estimate with confidence…
- A First-in-human Study of Single Doses of PF-07328948 Which is Given to Healthy Adult Participants: Complete Statistical AnalysisIndependent statistical analysis of A First-in-human Study of Single Doses of PF-07328948 Which is Given to Healthy Adult Participants: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- A Fixed-Sequence, Drug-Drug Interaction Study Between Multiple Oral Doses of Inarigivir Soproxil and a Single Oral Dose of Midazolam in Healthy Subjects: Complete Statistical AnalysisIndependent statistical analysis of A Fixed-Sequence, Drug-Drug Interaction Study Between Multiple Oral Doses of Inarigivir Soproxil and a Single Oral Dose of Midazolam in Healthy Subjects: primary endpoint results, effect estimate with…
- A Folinic Acid Intervention for Autism Spectrum Disorders: Complete Statistical AnalysisIndependent statistical analysis of A Folinic Acid Intervention for Autism Spectrum Disorders: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT01602016).
- A Follow-On Study of Donanemab (LY3002813) With Video Assessments in Participants With Alzheimer’s Disease (TRAILBLAZER-EXT): Complete Statistical AnalysisIndependent statistical analysis of A Follow-On Study of Donanemab (LY3002813) With Video Assessments in Participants With Alzheimer's Disease (TRAILBLAZER-EXT): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- A Gene Therapy Study for Homozygous Familial Hypercholesterolemia (HoFH): Complete Statistical AnalysisIndependent statistical analysis of A Gene Therapy Study for Homozygous Familial Hypercholesterolemia (HoFH): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT02651675).
- A Gene Transfer Therapy Study to Evaluate the Safety of SRP-9004 (Patidistrogene Bexoparvovec) in Participants With Limb-Girdle Muscular Dystrophy, Type 2D (LGMD2D): Complete Statistical AnalysisIndependent statistical analysis of A Gene Transfer Therapy Study to Evaluate the Safety of SRP-9004 (Patidistrogene Bexoparvovec) in Participants With Limb-Girdle Muscular Dystrophy, Type 2D (LGMD2D): primary endpoint results, effect estimate with…
- A Home-based Training Program for Elderly Patients With Dementia: Complete Statistical AnalysisIndependent statistical analysis of A Home-based Training Program for Elderly Patients With Dementia: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT02667951).
- A Long Term Follow up Administration Study of L059 (Levetiracetam) in Epilepsy Patients With Partial Onset Seizures: Complete Statistical AnalysisIndependent statistical analysis of A Long Term Follow up Administration Study of L059 (Levetiracetam) in Epilepsy Patients With Partial Onset Seizures: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration,…
- A Long Term Safety Study to Test the Combination of Aliskiren/ Amlodipine / Hydrochlorothiazide in Participants With Essential Hypertension: Complete Statistical AnalysisIndependent statistical analysis of A Long Term Safety Study to Test the Combination of Aliskiren/ Amlodipine / Hydrochlorothiazide in Participants With Essential Hypertension: primary endpoint results, effect estimate with confidence interval, sample-size…
- A Long-term Efficacy and Safety Study of Tramadol Hydrochloride Plus Acetaminophen (JNS013) in Japanese Participants With Chronic Pain: Complete Statistical AnalysisIndependent statistical analysis of A Long-term Efficacy and Safety Study of Tramadol Hydrochloride Plus Acetaminophen (JNS013) in Japanese Participants With Chronic Pain: primary endpoint results, effect estimate with confidence interval, sample-size planning…
- A Long-Term Extension Study of WA22762 to Evaluate Safety and Efficacy of Subcutaneous Tocilizumab in Participants With Moderate to Severe Rheumatoid Arthritis (RA).: Complete Statistical AnalysisIndependent statistical analysis of A Long-Term Extension Study of WA22762 to Evaluate Safety and Efficacy of Subcutaneous Tocilizumab in Participants With Moderate to Severe Rheumatoid Arthritis (RA).: primary endpoint results, effect estimate…
- A Long-term Follow-up Study (ZOE-LTFU) of Two Studies 110390 (ZOSTER-006) and 113077 (ZOSTER-022) to Assess the Efficacy, Safety, and Immunogenicity Persistence of GSK Biologicals’ Herpes Zoster Subunit (HZ/su) Vaccine and Assessment of 1 or 2 Additional Doses in Two Subgroups of Older Adults: Complete Statistical AnalysisIndependent statistical analysis of A Long-term Follow-up Study (ZOE-LTFU) of Two Studies 110390 (ZOSTER-006) and 113077 (ZOSTER-022) to Assess the Efficacy, Safety, and Immunogenicity Persistence of GSK Biologicals' Herpes Zoster Subunit (HZ/su)…