65,437 trials
Diabetes Mellitus, Non-Insulin-Dependent
Primary: Absolute Change From Baseline in Haemoglobin A1c (HbA1c) — -1.19; -1.59; -1.61 (%)
Low Back Pain
Primary: Difference in the Proportion of Primary Outcome Successes Between Treatment Groups — 27; 9 participants — p=<0.00001
Hearing Impairment
Primary: Change in Mean Aided Word Recognition Scores (WRS) When Compared to the Baseline Unaided Condition. — 37.6 percentage of words correctly identified — p=<0.0001
HIV · AIDS · Medication Adherence
Primary: Antiretroviral Therapy (ART) Adherence (Self-reported 3-day Recall Measure) — 142; 139; 6; 12 participants
Circumference Reduction
Primary: Change in Combined Circumference Measurements — -5.36 inches — p=<.0001
Anorexia Nervosa
Primary: Change in Eating Disorder Inventory-2 Drive for Thinness Subscale (DT) — 1.36; 3.93 units on a scale
Smoking
Primary: Maximum Concentration (Cmax) of Nicotine Following Single Use of mTHS, mCC and NRT — 10.70; 12.09; 7.64; 7.52 ng/mL
Non-small Cell Lung Cancer
Primary: Progression Free Survival (PFS) Rate as Per Investigator Local Review Measured Using RECIST 1.1 of Patients at Week 12 — 23.3; 20.0 Percentage of participants
Contraception
Primary: Expulsion Rate — 9 participants
Acute Heart Failure
Primary: Evaluation of Mean Urine Output Volume During the Infusion Period — 2505; 2140 mL — p=0.04
Carcinoma, Squamous Cell of Head and Neck
Primary: Progression Free Survival (PFS) Time — 82 days
Hypertension
Primary: Percentage of Participants With a Clinical or Laboratory Adverse Experience — 33.3; 53.8; 41.7; 61.5 Percentage of participants
Symptomatic Gastroesophageal Reflux Disease (sGERD)
Primary: Mean Percentage of Diary-Recorded Heartburn-Free Days at Week 4 — 21.23; 41.14 Percentage of Days
Paroxysmal Atrial Fibrillation
Primary: The Incidence of Early Onset Primary Adverse Events — 5.5 percentage of participants
Glioma · Low-grade Glioma · Astrocytoma
Primary: Overall Response — 2; 21 participants