65,437 trials
Vaginal Infection
Primary: Clinical Cure as Assessed by the Investigator at the Test-of-cure Visit — 47; 25 Participants — p=0.002
Neuroendocrine Tumors · Pancreatic Neoplasms
Primary: Objective Response Rate — 3; 14 Participants
Postoperative Nausea and Vomiting
Primary: Number of Participants With Nausea and/or Vomiting — 10; 26 Participants — p=0.003
Breast Surgery
Primary: Numeric Rating Scale Pain Scores — 3.0; 0 score on a scale — p=0.0011
Postoperative Pain · Endodontic Disease · Obturation
Primary: Visual Analogue Scale (VAS) — 4.06; 2.68; 2.41; 2.27 score on a scale
Attention Deficit Disorder With Hyperactivity
Primary: Test of Variables of Attention-Attention Performance Index (Change From Baseline to Posttreatment) — 0.93; 0.03 z-score
Leukemia, Lymphocytic, Chronic, B-Cell
Primary: Recommended Phase 2 Dose of BI 836826 in Combination With Ibrutinib
Heart Failure
Primary: Exercise Capacity as Measured by Peak Oxygen Uptake (Peak VO2) — 9.1; 9.8 mL/kg/min — p=0.053
Human Immunodeficiency Virus · Coronary Artery Disease
Primary: Coronary Endothelial Function as Assessed by Percent Coronary Artery Area Change With Isometric Handgrip Exercise — 5.6 percent change in coronary artery area
Pulmonary Disease, Chronic Obstructive
Primary: Change From Baseline in Lung Cathelicidin Level at 8 Weeks — -65.5 pg/mL — p=0.21
Depression
Primary: Change From Baseline on Symptoms of Depression Questionnaire (SDQ) — 3.7; 3.7; 3.5; 3.5 score on a scale — p=0.46
Colorectal Cancer
Primary: Progression-Free Survival (PFS) — 9.99; 11.60; 7.13; 7.36 months — p== 0.872
Malignant Glioma
Primary: Six-month Progression-free Survival (PFS6) — 14.3; 5; 14.3; 40 percentage of participants
Malaria
Primary: Number of Participants With P.Falciparum Blood Stage Infection — 0; 0; 0; 0 Participants
Nonalcoholic Steatohepatitis (NASH)
Primary: Percentage of Participants Experiencing Treatment-Emergent Adverse Events — 70.6; 71.4; 61.5 percentage of participants