12,372 trials
Chronic Schizophrenia
Primary: Relapse of Psychotic Symptoms — 29; 21 participants
Larynx Disease
Primary: Post Nasal Drainage Symptom Response — 55; 3.5; 50; 5 Scores on a Scale — p=.01
Dental Fluorosis · Dental Caries
Primary: Evaluation of the Concentration of Fluoride Incorporated Into the Biofilm Done 6 Months After Initiation of Dentifrices Use. — 0.80; 1.32; 1.74 mmol/kg — p=<0.05
Cystic Fibrosis
Primary: Absolute Mean Change From Baseline in Percent Predicted Forced Expiratory Volume in 1 Second (FEV1) Through Week 24 — -0.2; 10.4 percent of predicted volume (L)…
Cystic Fibrosis
Primary: Absolute Change From Baseline in Percent Predicted Forced Expiratory Volume in 1 Second (FEV1) Through Week 24 — 0.1; 12.6 percent of predicted volume (L) — p=<0.0001
Hepatitis C
Primary: The Percentage of Subjects Achieving Undetectable Hepatitis C Virus (HCV) Ribonucleic Acid (RNA) at 24 Weeks After Completion of Drug Administration (SVR, Sustained…
Hepatitis C
Primary: The Percentage of Subjects Achieving Undetectable Hepatitis C Virus (HCV) Ribonucleic Acid (RNA) at 24 Weeks After Completion of Drug Administration (SVR, Sustained…
Chronic Hepatitis C
Primary: The Percentage of Subjects Achieving Undetectable Hepatitis C Virus (HCV) Ribonucleic Acid (RNA) at 24 Weeks After Completion of Drug Administration (SVR, Sustained…
Pain
Primary: Time-weighted Sum of Pain Relief Rating With Pain Intensity Difference From 0 to 6 Hours (SPRID 0-6) — 2.8; 20.0; 17.1 units on a scale — p=<0.001
Psychotic Depression
Primary: Depression and Psychosis Response Rate — 62.5 percent of participants
Pain
Primary: Time-weighted Sum of Pain Relief Rating and Pain Intensity Difference From 0-3 Hours (SPRID 0-3) for Ibuprofen Sodium Versus Placebo Tablet — 11.2; 10.8 Units on a scale…
Type 2 Diabetes Mellitus
Primary: Change in HbA1c From Baseline to Week 30 — -1.87; -1.54 percentage of total hemoglobin — p=0.0023
Multiple Sclerosis · Spasticity
Primary: Incidence of Adverse Events as a Measure of Patient Safety — 126 participants
Pain
Primary: Time-weighted Sum of Pain Relief Rating and Pain Intensity Difference From 0-8 Hours (SPRID 0-8) — 5.4; 29.8 Units on a scale — p=<0.001
Postoperative Cognitive Dysfunction
Primary: Mini Mental State Examination (MMSE) — 27; 26.769 scores on a scale — p=0.678