65,437 trials
Instability, Joint
Primary: Clinical Success at 6 Months — 56 Participants
Tuberculosis, Multidrug-Resistant
Primary: Treatment Success Rate — 60; 54 Participants
Healthy Volunteers
Primary: AUC0-last — 146000; 134000; 138000 day*ng/mL
Septic Shock
Primary: Total Vasopressor Dose — 13.7; 13.1; 13.2; 11.3 mg
Vitamin B1 Deficiency · Thiamine Deficiency
Primary: Maximum Concentration (Cmax) of Thiamine in Plasma Between the Combination Arm(s) and Single Agent Arm — 15; 32 nM
Asthma
Primary: Number of Treatment-emergent Adverse Events and Serious Adverse Events — 19; 17; 12; 9 adverse events
Orthodontic Retainers · Clinical Trial
Primary: Arch Width — 36.9; 37.65; 44.61; 46.31 milimeters
Breastfeeding
Primary: Breastfeeding Duration 1 — 674; 639 Participants — p=0.08
Huntington's Disease
Primary: Change From Baseline in the Following Clinical Endpoints at 3, 9, and 15 Months: cUHDRS, TFC, TMS, SDMT, SWR Test and IS — 0.19; -0.12; -0.76; -0.24 Scores on a scale
Primary IgA Nephropathy
Primary: Ratio of Urine Protein to Creatine Ratio (UPCR) at 9 Months Compared to Baseline — 0.67; 0.69 ratio
Uncomplicated Plasmodium Falciparum Malaria
Primary: AUC0-21d — 144; 205; 259; 318 hr*ug/mL
Anhedonia · Depression
Primary: Non-social (Monetary) Reward Response (Reward Learning and Sensitivity) — .563; .307; .309; .366 response bias — p=.16
Endometrial Cancer · Endometrial Carcinoma · Neoplasms, Endometrial
Primary: Safety as Measured by Any Grade Treatment Related Adverse Events Experienced by ≥ 2 Patients — 10; 9; 8; 8 Participants
Hip Osteoarthritis
Primary: Surgeon Participant Intra-operative Motion Analysis — 171,967; 172,258; 150,505 Movement counts
Healthy Volunteers
Primary: Maximum Observed Plasma Concentration (Cmax) of Nemolizumab — 8.00; 7.51 micrograms per milliliter (mcg/mL)