65,437 trials
Intravaginal Ring Use
Primary: USPE Scale Scores — 3.73; 3.63; 1.85; 2.02 score on a scale
Covid19
Primary: Substudy Analysis Cohorts — 18; 21; 25; 21 Participants
Liver Transplant Surgery
Primary: Incidence of Postoperative Residual Weakness in the Recovery Room — 2; 0 Participants
Substance Use · Substance Abuse · Substance-Related Disorders
Primary: Proportion of Patients That Had a Universal Screen Positive and Received SBIRT (Screening, Brief Intervention, or Referral to Treatment) — 1189; 1144 Participants — p=0.20
Asthma in Children
Primary: Total Number of Treatment Days in a Medical Setting (Hospital, Emergency Department (ED), Clinic) — 1.97; 2.67 days
Melanoma · Carcinoma, Hepatocellular · Colorectal Neoplasms
Primary: Phase 1b Part: Number of Participants With Dose-limiting Toxicities (DLTs) — 0; 0 Participants
Dementia · Cognitive Impairment
Primary: Change in Center for Epidemiological Studies Depression Scale (CES-D) From Baseline — 7.04; 6.09 score on a scale — p=0.020
Neovascular Age-related Macular Degeneration
Primary: Incidence and Severity of Ocular Adverse Events in the Study Eye, With Severity Determined According to Adverse Event Severity Grading Scale — 188; 207; 16; 114…
Rheumatoid Arthritis
Primary: Change in Tissue Sodium — 17.1; 16.7 mmol/L — p=0.55
Actinic Keratosis
Primary: Treatment Efficacy Based on Participant AK Lesion Clearance — 59; 34; 43; 76 percentage of AK lesions
Relapsing Multiple Sclerosis
Primary: Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Treatment-emergent Serious Adverse Events (TESAEs) — 17; 17; 24; 20 Participants
Cough · Superior Laryngeal Nerve Block · Neurogenic Cough
Primary: Change in Cough Severity — 13.15; 9.54 LCQ scores (baseline to 3 months)
Dementia
Primary: OSHH Program Effectiveness of Educating Parents at 1-week and 3-months After the Intervention Using ASK-AD 7 — 5.14; 5.28; 5.41; 5.62 score on a scale
Persistent Atrial Fibrillation · Atrial Fibrillation
Primary: Primary Safety Events — 16 participants
Nipah Virus Infection
Primary: Number of Participants Reporting Local Reactogenicity Signs and Symptoms Within 7 Days of Product Administration — 1; 1; 0; 4 Participants