65,437 trials
Hepatitis
Primary: Number of Outcomes From Pregnancies With Reported Exposure Within 28 Days of Last Menstrual Period — 0; 0; 0; 0 Pregnancy Outcomes
Infection, Human Immunodeficiency Virus · HIV Infections
Primary: Assessment of Plasma CAB Pharmacokinetic (PK) Parameter: Area Under the Concentration-time Curve Over One Dosing Interval (AUC [0 to Tau]) — 103.978; 81.715 Microgram *…
Nausea · Emesis
Primary: Number of Participants With Nausea 1 Hour After Post-anesthesia Care Unit (PACU) Admission — 1; 0; 1; 14 Participants
Infant, Newborn
Primary: Number of Transfusions During Hospitalization — 1.2; 1.2; 2.4 number of transfusions
Aortic Aneurysm, Abdominal
Primary: Freedom From Aneurysm-related Mortality Rate (ARM) at 5 Years (1826 Days) — 0.989 Proportion of Surviving
Surgical Port Site Hernia
Primary: Time Taken to Complete Closure — 36.8; 48.9 seconds
Atherosclerosis · Peripheral Vascular Disease · Claudication
Primary: Device Success — 100.0 percentage of devices
Leukemia · Lymphoma · Myeloma
Primary: Maximum Tolerated Dose — 6800 mmol-min/L
Renal Insufficiency
Primary: Number of Patients With Moderate to Severe Renal Impairment Who Develop Nephrogenic Systemic Fibrosis (NSF) After Administration of Dotarem — 0 Participants
Hypertension, Resistant to Conventional Therapy
Primary: Changes of 24h-mean Systolic BP Assessed by Ambulatory Blood Pressure Monitoring (ABPM) — 21.1; 10.3 mmHg — p=0.045
Iron-refractory, Iron-deficiency Anemia (IRIDA)
Primary: Pharmacokinetics (PK) of Total Iron From Triferic Administered Orally in Adult Healthy Patients: Cmax — 140; 62.0; 32.4; 51.9 microgram/deciliter
Schizophrenia · Bipolar Disorder · Major Depression
Primary: Patient Experience of Medication Treatment (PEMM) — 3.009; 3.007; 2.6; 3.09 Units on a scale — p=<0.0001
Infections, Meningococcal · Meningococcal Vaccines
Primary: Percentage of Subjects With Serum Bactericidal Assay Using Baby Rabbit Complement Against Meningococcal Serogroups A, W-135 and Y (rSBA-MenA, rSBA-MenW-135 and rSBA-Y)…
Neoplasms
Primary: Number of Participants With Dose Limiting Toxicities (DLT) — 0; 0; 3; 2 participants
Herpes Zoster Disease
Primary: Number of Participants Who Received the Herpes Zoster Vaccine — 500; 2089 Participants