65,437 trials
Pain
Primary: Number of Participants Who Requested Analgesia During the Active Phase of Childbirth — 37; 35 Participants
Healthy
Primary: Area Under the Concentration-time Curve of the Analyte in Plasma at Steady State Over a Uniform Dosing Interval τ (BI 425809 + Memantine : BI 425809) — 9029.04; 8559.78…
Stroke · Hemiparesis
Primary: Wolf Motor Function Test Performance Time (WMFT) — 3.6; 2.9; 3.1 log (seconds) — p=0.64
Coronavirus · Acute Respiratory Infection · SARS-CoV Infection
Primary: COVID Outcomes Scale Score on Study Day 15 (14 Days After Randomization) — 6; 6 score on a scale
Recurrent Non-Small Cell Lung Carcinoma · Stage IV Non-Small Cell Lung Cancer
Primary: 2-year Overall Survival Rate — 67; 70 percentage of participants — p=0.44
Covid-19
Primary: Number of Participants Who Achieved Clinical Response by Day 15 — 7; 7; 4 Participants
Urolithiasis
Primary: Adherence to Intervention Assessed by Study Completion — 27 Participants
Sickle Cell Disease
Primary: Scores on Behavioral Activation Measure at Baseline and 6 Weeks (Post-treatment) — 68.48; 69.13; 76.57; 68.82 score on a scale — p=.09
HIV · Hepatitis C
Primary: Simeprevir AUC Pharmacokinetics — 30946; 30333 ng*h/mL
Retinal Vein Occlusion
Primary: The Primary Outcome is the Comparison Between the Minocycline and Placebo Groups of the Mean Change in Best-corrected Visual Acuity (BCVA) in the Study Eye at 12 Months…
Depressive Disorder, Major · Depressive Disorder, Treatment-Resistant
Primary: Incidence of Treatment Emergent Adverse Events (AEs) [Safety and Tolerability] — 9; 15; 12; 0 Participants
Visual Acuity
Primary: Monocular Contact Lens-corrected Distance Visual Acuity (Per-Protocol Population) — -0.111; -0.109; -0.115; -0.118 logMAR
Breast Cancer
Primary: Percentage of Participants With Disease-free Survival (DFS) — 78.97; 83.37 Percentage of participants — p=0.175
Pain, Chronic · Cancer
Primary: Improvement of Pain. — 3 score on a scale (0-10)
Small Cell Lung Cancer · Small Cell Lung Cancer Extensive Stage
Primary: Phase I - Recommended Phase II Dose (RP2D) of 177Lu-DOTA0-Tyr3-Octreotate — 7.4 GBq