65,437 trials
Dental Research · Pharmaceutical Preparations, Dental
Primary: Decrease Time of Oral Pain — 9; 9; 5; 4 score on a scale
Non-Small Cell Lung Cancer
Primary: Overall Response Rate (ORR) Per RECIST 1.1 — 0.395; 0.404 proportion of participants — p=0.2176
Generalized Anxiety Disorder
Primary: Change From Baseline in the HAM-A Total Score at Week 8 — -9.28; -9.35 score on a scale — p=0.917
Xerostomia
Primary: Number of Participants With Adverse Events as a Measure of Safety — 0; 0 participants
Safety · Adverse Event Following Immunisation · Birth Outcomes
Primary: Number of Pregnant Women Vaccinated With RIV4 Versus IIV4 With Adverse Birth Outcomes — 17; 21 Participants — p=<0.0001
Molluscum Contagiosum
Primary: Complete Clearance of All Treatable MC at Week 12 — 61; 25 Participants
Chronic HIV Infection
Primary: Number of Participants With Viral Suppression — 289; 283 participants — p=0.55
Pancreatic Cancer · Pancreas Adenocarcinoma · Advanced Pancreatic Cancer
Primary: Progression- Free Survival at 6 Months From Initiation of Trial Treatment — 0; 2 Participants — p=.31
Graft Versus Host Disease · Leukemia · Myelodysplastic Syndromes
Primary: Response to Therapy — 1; 0; 27; 4 Participants
Multiple Sclerosis
Primary: Change in the Modified Fatigue Impact Scale (MFIS) Score — -15.2; -16.0; -17.3 score on a scale — p=0.3451
High Grade Malignant Neuroendocrine Carcinoma (Diagnosis)
Primary: Overall Response Rate (ORR) — 7; 5 percentage of participants
Intravenous Drug Usage · HIV/AIDS
Primary: Composite PWID Score (Service Access, Risk Behaviors, Adverse Outcomes) — 5.34; 5.64 units on a scale — p=0.125
Osteoarthritis
Primary: Change From Baseline in T1ρ Relaxation Time — 2.1; 13.3 milliseconds
Leber's Congenital Amaurosis
Primary: Frequency and Severity of Ocular Adverse Events in the Treatment and Contralateral Eyes — 6; 5 Participants
Breast Cancer
Primary: Feasibility of the Intervention Trial - Enrollment — 96.97 percent of eligible study candidates