65,437 trials
Attention Deficit Disorder With Hyperactivity
Primary: NCBRF-TIQ D-Total Score — 43.5; 42.1; 24.9; 25.9 units on a scale
Pheochromocytoma · Paraganglioma
Primary: MTD of Ultratrace Iobenguane I 131 — 8 mCi/kg
Diabetes · Diabetes Mellitus, Type 2
Primary: Change From Baseline in Glycosylated Haemoglobin (HbA1c) (%) — -0.99; -0.07 percentage of glycosylated haemoglobin
Platinum-sensitive Ovarian Cancer, Second-line, Third-line, or Fourth-line
Primary: Number of Participants With Drug-related Adverse Events (AEs) of Grade 3 or Higher — 20 Participants
Infertility
Primary: Number of Participants of Severe Ovarian Hyperstimulation Syndrome — 2; 11 participants
Port Wine Stains
Primary: Blanching of Port Wine Stain Birthmark — 16 participants
Alveolar Bone Loss
Primary: Bone Height — 12.2 millimeters
Attention Deficit Hyperactivity Disorder (ADHD)
Primary: SKAMP-Combined Scores — 10.0; 17.8 units on a scale — p=<0.0001
Primary Peritoneal Carcinoma · Stage III Ovarian Cancer · Stage IV Ovarian Cancer
Primary: Overall Survival — 0.35; 0.34; 0.39; 0.34 Proportion of participants
Astigmatism
Primary: Participant's Subjective Rating for Lens Initial Comfort — 6.9; 7.4; 8.0; 8.9 units on a scale
Solid Tumours
Primary: Cmax of Olaparib — 7.227; 9.081; 9.977 μg/mL
Hepatitis C, Chronic
Primary: Number of Participants With Virologic Response Defined as >= 3 Log Drop in Viral Load From Baseline at Day 28 With no Evidence of Virologic Rebound During These 28 Days…
Type 3 Von Willebrand's Disease
Primary: Centralized Factor VIII (FVIII) Procoagulant Activity (FVIII:C) Laboratory Test for Type 3 Von Willebrand's Disease (VWD3) Diagnosis — 2.42 IU/dL
Actinic Keratoses
Primary: Lesion Response — 89.2; 92.8 percentage of lesions complete response — p=0.0345
Pain, Postoperative
Primary: Total Opiate Requirement — 1.19; 1.01 mg/kg