65,437 trials
Polyarticular Juvenile Idiopathic Arthritis
Primary: Number of Participants With Adverse Events — 6; 1; 1 participants
Chronic Plantar Fasciitis
Primary: Responders Rate at Week 6 (Pain While Moving) — 25.0; 5.0 Percentage of participants — p==0.182
Obesity
Primary: Fat Reduction in Treatment Zone as Measured in Inches Lost — 3.5 inch
Hyperkalemia
Primary: Incidence of Pre-dialysis HK After the LIDP in <3K Dialysate Patients — 50; 37 Percent of participants
Pancreatic Adenocarcinoma
Primary: Safety Run-In Part: Number of Subjects With Dose Limiting Toxicities (DLTs) — 0; 0; 0; 0 subjects
Diabetes Mellitus, Type 1
Primary: Percent of Sensor Glucose Readings Between 70-180 mg/dL — 46.9; 73.1 percentage of time in range
Hypercholesterolemia · Hydroxy-methylglutaryl-coenzyme A (HMG Co-A) Reductase Inhibitors Adverse Reaction
Primary: Morisky Medication Adherence Scale (MMAS) Score — 6.8; 6.9; 6.8; 7.1 units on a scale — p=0.96
Multiple Myeloma
Primary: Effect of Drug Combination on Multiple Myeloma — 2; 9; 9; 5 participants
Asthma · Efficacy · Safety
Primary: Efficacy of AZD7594 by Assessment of the Change From Baseline in Morning Trough Forced Expiratory Volume in 1 Second (FEV1) on Day 15 — 0.08639; 0.05948; 0.1355; 0.05948…
Forehead Rhytides · Glabellar Rhytides
Primary: Percentage of Subjects With ≥2-Grade Improvement From Baseline on Both the Investigator's and Subject's Facial Wrinkle Scale (FWS) Ratings of Forehead Line Severity at…
Recurrence · Smoking Cessation · Substance-Related Disorders
Primary: Days to Relapse — 9.1; 16.4 days
Lung Cancer · Unspecified Adult Solid Tumor, Protocol Specific
Primary: Number of Patients Experiencing a Dose-limiting Toxicity (Phase I) — 3; 0 Participants
Spinal Cord Injury · Bone Loss · Osteoporosis
Primary: Bone Mineral Density BMD of the Total Hip as Assessed by DXA. — 0.66; 0.63; 0.64; 0.65 g/cm^2 — p=0.84
Uterine Cervical Neoplasms
Primary: Proportion of Patients Who Receive a Pap Test at End of Follow up — 44; 50; 53; 59 Participants
Full Thickness Rotator Cuff Tear
Primary: Number of Participants With Device Associated Adverse Events — 4 Participants