65,437 trials
Pharmacokinetics
Primary: Maximum Plasma Concentration (Cmax) — 12.2; 1.77 ng/ml
Bone Marrow Edema
Primary: Reduction of the Edema Area — 64.53; 23.97 percentage of edema volume — p==0.006
Locally Advanced Breast Cancer · Metastatic Breast Cancer
Primary: Percentage of Patients Without Disease Progression — 7; 8 Participants
Presbycusis
Primary: Hearing Aid Benefit as Measured by the Glasgow Hearing Aid Benefit Profile (GHABP) — 3.68; 3.55; 3.63 score on a scale
Palliative Care · Dementia
Primary: Adherence to Skilled Nursing Facility (SNF)-PCC Recommendations
Caregiver Burnout
Primary: Change in Pre-post Scores on the Perceived Stress Scale (PSS) — 4.75 score on a scale
Genetic Testing
Primary: Participant Satisfaction With How Educational Information is Presented in the Decision Aid — 1; 3; 29; 55 Participants
Post-traumatic Headache · PTSD
Primary: Headache-related Disability Scores on the Headache Impact Test 6 (HIT-6) — 66.1; 66.1; 65.2; 61.9 score on a scale — p=<0.001
End-Stage Renal Disease
Primary: Primary Safety Endpoint — 16.1; 11.6 Adverse Events per 100 Treatments
HIV Infections · Behavioral Symptoms · Depression
Primary: Total Number of Participants Who Were Eligible and Enrolled (Intervention Feasibility) — 75 Participants
Obesity · Weight Loss · Diabetes Mellitus
Primary: Weight Loss of ≥15% From Baseline (Complete Cases) — 51; 6 Participants — p=<0.001
Coagulation; Intravascular
Primary: Activated Clotting Time — 116; 113 seconds
Diabetes Mellitus, Type 2
Primary: Quantify the Percentage Change in Basal Circulating sRAGE After 12-weeks of Supervised Aerobic Exercise Training. — 24.5; 0.5 Percent Change in sRAGE
Healthy
Primary: Cmax — 4.880; 4.680; 3.860 (μg/mL)
Type 2 Diabetes Mellitus
Primary: Number of Participants With Treatment-emergent Adverse Events (All Causalities) — 5; 7; 6; 0 Participants