65,437 trials
Healthy
Primary: Area Under the Plasma Concentration-Time Curve From Time Zero to Last Measurable Concentration (AUC0-t) of L-Praziquantel (L-PZQ) — 441.53; 547.41; 460.25 Hour*nanogram…
Hypercholesterolemia With Type2DM
Primary: Proportion of Patients Achieving LDL- C<100mg/dL — 61; 54 Participants
Malignant Pleural Mesothelioma
Primary: Overall Survival (OS) — 8.5; 8.0 months — p=0.58
HIV Infections
Primary: Termination From Treatment Due to a Suspected Adverse Drug Reaction (SADR) — 1; 0; 10; 4 Participants
Head Cancer · Neck Cancer · Pain
Primary: Change in Pain Intensity in Head/Neck Cancer Area: 10cm Visual Analog Scale (VAS) — -1.4; -0.6; 0.1 change units on a VAS scale
Prostate Cancer
Primary: Cancer Detection by Targeted and Standard Biopsy Approaches
Attention-deficit/Hyperactivity Disorder
Primary: Number of Dose Changes Required Per Protocol — 1.79; 1.61 Number of Increases
Atherosclerosis · Diabetes · Coronary Artery Disease
Primary: Mean IL-1 Beta Release From Peripheral Blood Mononuclear Cells During Refeeding After 24 Hour Fast — 582; 794 mg/dL
Fallopian Tube Clear Cell Adenocarcinoma · Fallopian Tube Endometrioid Adenocarcinoma · Fallopian Tube Mucinous Adenocarcinoma
Primary: Proportion of Participants With Objective Response — 0.196 Proportion of participants
Osteoarthritis (OA)
Primary: PROMIS Pain Interference — 19.0; 19.1; 18.0; 17.5 score on a scale
Environmental Tobacco Smoke · Smoking Cessation
Primary: Feasibility as Assessed by Number of Participants Who Accepted NRT Patches From Research Staff. — 13 Participants
Epidural Anesthesia · Spinal Ultrasound · Obesity
Primary: Time for Epidural Placement — 9.0; 6.2 minutes
Head and Neck Carcinoma · Radiation-Induced Dermatitis
Primary: Radiation Dermatitis — 34; 36 Participants — p=.8872
Erythropoietic Protoporphyria
Primary: Time in Direct Sunlight Between 10:00-15:00 on Pain-free Days — 8.25; 0.75 Hours
Complicated Intra-abdominal Infection · Complicated Urinary Tract Infection
Primary: Percentage of Participants Experiencing ≥1 Adverse Events (AE) — 74.1 Percentage of Participants