65,437 trials
Human Immunodeficiency Virus · Cardiometabolic Risk
Primary: Number of Eligible Participants Refusing to Participate. — 0 Participants
Cutaneous T-Cell Lymphoma
Primary: Overall Response Rate of Participants Using the Modified Severity-Weighted Assessment Tool (mSWAT) — 16.7; 20.3; 18.5 percentage
Parkinsons Disease
Primary: Change in the Mean Daily Overactive Bladder-Symptom Composite Score. — -3.2; -8.9 units on a scale
Cytokine Release Syndrome (CRS) in Patients With COVID-19-induced Pneumonia
Primary: Participants Who Survived Without Requiring Invasive Mechanical Ventilation From Day 3 to Day 29, Primary Analysis — 198; 191 Participants — p=0.2874
Mitral Valve Disease
Primary: Technical Success at Exit From the Cath Lab. — 23; 20; 30 Participants
Multiple Sclerosis
Primary: Percentage of PP Exercises Completed by Subjects — 93; 93 percentage of exercises completed
Suicidal Ideation · Suicide Attempt · Mental Health
Primary: Acceptability of Intervention — 14; 16 Participants
Diabetes Mellitus, Type 1
Primary: Treatment Satisfaction: Accu-Chek® Micropump System vs. MDI, Measured by the Difference in the Diabetes Technology Questionnaire (DTQ) Total Change Score — 105.9; 94.8…
Schizophrenia
Primary: Prepulse Inhibition (PPI) — 22.629; 41.162; 50.626; 50.626 % inhibition of startle
Spinal Metastases
Primary: Phase III: Complete Pain Response at 3 Months Post-radiation — 16; 40; 29; 20 Participants — p=0.0002
Myelodysplastic Syndrome · Iron Overload
Primary: Number of Participants Reporting Adverse Events — 171 Participants
Asthma
Primary: FEV1 Area Under the Curve Between 0 and 12 h [AUC(0-12h)], Normalized by Time -- Change From Baseline to Post Dose Day 14 — 0.174; 0.221; 0.197; 0.231 Litres — p=<0.001
Alzheimer's Disease · Psychosis · Agitation
Primary: Change in Neuropsychiatric Inventory (NPI) Agitation/Aggression Domain Score — 3.2; 2.5 score on a scale — p=0.53
Covid19
Primary: Average Days in COVID-19 Symptoms by Type of Therapy in the UMF 20 and UMF 13 of the IMSS. — 7; 7; 2; 2 days — p=0.05
Advanced Solid Tumors · Acute Myeloid Leukemia
Primary: Number of Participants With Adverse Events — 2; 3; 3; 1 Participants