12,372 trials
Acute Respiratory Infection
Primary: Fever Duration (With a Superiority Cut-off Level δ=-0,52 Days) — 2.04; 2.26 day — p=<0.05
Early Breast Cancer
Primary: Trough Serum Concentration (Ctrough) of Pertuzumab During Cycle 7 (Pre-Dose Cycle 8) — 72.4; 88.7 micrograms per millilitre (μg/mL)
Chronic Idiopathic Constipation
Primary: Complete Spontaneous Bowel Movement (CSBM) Response — 47; 56 Participants — p=0.016
Ankle Sprain
Primary: Visual Analogue Scale (VAS) Scores at Baseline and Post Treatment — 68.56; 69.03; 25.34; 25.78 score on a scale
Attention-Deficit Hyperactivity Disorder (ADHD)
Primary: Change From Baseline at Day 15 in , ADHD Symptoms as Measured by Mean Swanson,Kotkin,Agler,M-Flynn, Pelham Rating Scale(SKAMP)-Combined Score Obtained From an Average of…
Periodontitis · Periodontal Pocket · Diabetes Mellitus
Primary: Probing Depth — 0.44; 0.50 mm — p=<0.05
Acne
Primary: Percent Change From Baseline to Week 12 in the Number of Inflamed Lesions. — -74.2; -73.0; -30.6 percentage of change from baseline
Acute Lymphoblastic Leukemia · Adult B Lymphoblastic Lymphoma · Ann Arbor Stage I B Lymphoblastic Lymphoma
Primary: Disease Free Survival (DFS) in Average Risk (AR) Patients Based on the Methotrexate Dose Randomization — 95.05; 94.17 percent probability
Breast Cancer
Primary: Disease Free Survival (DFS) Benefit of Two Years Adjuvant Therapy With the COX-2 Inhibitor Celecoxib Compared With Placebo in Primary Breast Cancer Patients. — 91; 90…
Crohn's Disease
Primary: Percentage of Participants Achieving Clinical Remission at Week 52 — 34.3; 48.0 percentage of participants — p=0.008
Hypereosinophilic Syndrome
Primary: Number of Participants With Common (>=3%) Non-serious Adverse Events (AEs) — 34 Participants
Abscess
Primary: Number of Participants With Abscess Resolution — 11; 9 Participants
Depressive Disorder, Major
Primary: The Number of Participants With Treatment-Emergent Adverse Events (TEAEs) — 457 Count of Participants
Brain Stem Glioma · Cerebral Astrocytoma · Childhood Cerebellar Anaplastic Astrocytoma
Primary: Maximum Tolerated Dose (MTD) of Vorinostat — 230 mg/sq m
Lung Cancer
Primary: Progression Free Survival Rate (PFSR) at 6 Months — 0.76; 0.79 Proportion of Participants