65,437 trials
Stroke · Stroke, Ischemic · Stroke Hemorrhagic
Primary: Incidence of Treatment-Emergent Adverse Events — 2; 0 adverse events
Low Vision
Primary: Activity Inventory — 0.44; 0.43 logit — p=0.73
Pain · Depressive Symptoms · Frailty
Primary: Pain Intensity as Assessed by the Patient Reported Outcomes Measurement Information System (PROMIS) — 6.75; 7.29; 6.64; 7.00 score on a scale
Breast Cancer
Primary: Progression-Free Survival (PFS) — 30.6 Months
Acute Orthopedic Injury
Primary: Feasibility of Recruitment Among All Patients — 210 Participants
Psychological Distress · Cardiometabolic Syndrome
Primary: Rates of Recruitment and Retention — 24; 24; 23 Participants
Brain Neoplasms, Primary Malignant
Primary: Number of Participants With Dose Limiting Toxicities — 0; 0; 0; 0 Participants
Glioma · Glioblastoma Multiforme
Primary: Feasibility of Patient Treatment Compliance as Measured by Number of Participants Who Were at Least 80% Compliance With Assigned Administration Time — 17; 15 Participants
Advanced Solid Tumor · Lung Cancer · Pancreas Cancer
Primary: Safety and Tolerability Assessment of CNSI-Fe(II) — 0; 0; 1; 0 Participants
HIV Infections
Primary: Number of Participants Reporting Local Solicited Adverse Events Signs and Symptoms: Pain and/or Tenderness — 0; 0; 1; 5 Participants
Lower Extremity Acute Limb Ischemia · LE ALI
Primary: Target Limb Salvage Rate — 109 Participants
Opioid-use Disorder
Primary: Treatment Success Rate — 70; 67 Participants — p=0.7326
Radiation Dermatitis
Primary: Grade 3 or Higher Adverse Events — 9 Participants
Schizophrenia · Schizoaffective Disorder
Primary: Change in Cognition and Psychopathology Disorders as Measured on the MATRICS Consensus Cognitive Battery (MCCB) — 14.1; 14.3 units on a scale
Glabellar Lines
Primary: Number of Participants With Treatment-Emergent Adverse Events (TEAEs) — 7; 15; 9; 2 Participants