65,437 trials
Renal Cell Carcinoma · Kidney Cancer
Primary: Progression Free Survival (PFS) — 5.5 Months
Contraception
Primary: Pain at Time of IUD Insertion Using a 10 cm (100 mm) Visual Analog Scale (VAS) — 69; 66 units on a scale
Rett Syndrome
Primary: Adverse Events — 4; 4; 2; 17 Adverse events
Fatty Liver
Primary: Subcutaneous Fat in Steatosis Patients — 9.54; 10.48; 5.24; 4.09 cm^3
Pulmonary Disease, Chronic Obstructive
Primary: Percentage of Participants Preferring the Inhaler Based on the Number of Steps Needed to Take the COPD Medication — 73; 20; 7 Percentage of participants — p=<0.001
Lumbar Spinal Fusions
Primary: Patient Controlled Analgesia (PCA) Hydromorphone Usage — 44; 39 mL
Relapse Multiple Myeloma · Refractory Multiple Myeloma
Primary: Safety and Efficacy of High Dose Carfilzomib — 3; 13 Participants
Hypercholesterolemia
Primary: Percentage Change From Baseline in Low-Density Lipoprotein Cholesterol (LDL-C) — 7.6; -14.9; -40.5; -50.5 Percentage change
Carcinoma, Non-Small-Cell Lung
Primary: Confirmed Objective Response Rate (ORR) as Assessed by Investigator — 45.5; 57.3 percentage of participants
Hypercholesterolemia
Primary: Percent Change From Baseline in Low-density Lipoprotein Cholesterol (LDL-C) at Week 12 — -19.3; -44.0; -49.1; -55.6 Percentage Change — p=<0.001
Lymphoma, Large-Cell, Anaplastic · Carcinoma, Non-Small-Cell Lung
Primary: Recommended Phase 2 Dose (RP2D) of Brigatinib — NA mg
Cocaine-Related Disorders
Primary: Cocaine Use as Assessed by the Treatment Effectiveness Score (TES), Which is the Total Number of Cocaine-negative Urines During Treatment — 9.25; 6.09; 6; 4.91 number of…
Advanced Solid Tumors · Lymphomas
Primary: Maximum Plasma Concentration (Cmax) of Radiolabeled 14^C-Lenvatinib and Non-Radiolabeled Lenvatinib — 485.2; 426.8 ng/mL
Uveitis
Primary: Percentage of Participants With at Least 2-step Reduction in Vitreous Haze (VH) or Prednisone Dose <10 mg/Day at Week 16 — 30.0; 46.1 Percentage of participants — p=0.2354
Schizophrenia
Primary: Physical Examination Shift Table — 1; 1; 0; 0 Participants abnormal at end of study