65,437 trials
Schizophrenia
Primary: Average Number of CAE-S Sessions Attended by Those in the CAE-S Group After 12 Weeks — 4.89 Number of sessions attended
Chronic Pruritus in Adult Subjects With Notalgia Paresthetica (NP)
Primary: Percent Change From Baseline in Weekly Mean of the Daily 24-hour Worst Itch-Numeric Rating Scale (WI-NRS) Score at Week 4. — -44.37; -50.37 percentage of change from…
Asthma
Primary: Chest Wall Muscle Size — 95.49; 97.82; 87.98; 102.86 cm2
Caregivers · Technology
Primary: Number of Participants Who Agreed to Participate — 50 Participants
Sleep Apnea
Primary: PAP Adherence — 2.16; 0.87 hours per night — p=.0001
Ichthyosis
Primary: Change in Investigator Global Assessment (IGA) Score — 41.4; 44.9 percentage of responders — p=0.39
Acute Pain
Primary: Compared the Summed Pain Intensity From the End of Surgery to 48 Hours (SPI48) Between the High-dose XG005 Group and the Placebo Group Postoperatively. — 132.63; 285.99…
Asthma in Children
Primary: Mean Asthma Control Questionnaire Score — 2.7; 2.63; 0.98; 0.82 score on a scale
Covid19
Primary: Total Number of Participants Randomized Within Each Appendix — 1800; 1331; 1407; 1459 Participants
Upper GI Bleeding
Primary: Number of Participants With True Positive Results — 3 Participants
End-Stage Renal Disease · End-Stage Kidney Disease · Kidney Failure, Chronic
Primary: Time to First Arteriovenous Graft (AVG) Thrombosis Event — 23.80; 22.98; 30.17 events per 100 person-years — p=0.470
HIV · Hepatitis C · Substance Use Disorders
Primary: Feasibility Outcome: Number of Participants Who Are Enrolled and Complete the Baseline Study Assessment — 219 Participants
Advanced Solid Tumors · Triple Negative Breast Cancer · Ovarian Cancer
Primary: Objective Response Rate (ORR) Per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) by Investigator Assessment — 22.6; 25.8 Percentage of Participants
Dyslipidemia
Primary: Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) Level From Baseline to Week 12 — -31.19; -33.83; -41.09; -46.62 Percent Change (%) — p=< 0.001
Vitiligo
Primary: Proportion of Participants Achieving a ≥ 35% Improvement From Baseline in the Facial Vitiligo Area Scoring Index (F-VASI35) at Week 24 — 0.150; 0.053 Proportion of…