Clinical Trial Search

Primary: Number of Participants With Void Trial Failure Rate — 7; 11 Participants

Primary: Number of Patients Who Developed Postoperative Urinary Retention (POUR), Unable to Void a Volume Greater Than or Equal to 30ml/hr — 4; 5 Participants

Primary: Number of Participants With Postoperative Urinary Retention — 11 Participants

Primary: Number of Participants With Post Operative Urinary Retention — 23; 21 Participants

Primary: Number of Participants With Postoperative Urinary Retention — 14; 16 Participants

Primary: Number of Subjects With Urinary Retention — 15; 14 Participants

Primary: Number of Participants With Postoperative Urinary Retention After Pelvic Organ Prolapse Surgery (INTENT-TO-TREAT) — 30; 25 Participants

Primary: Number of Participants Considered to Have Passed Their Voiding Trial — 30; 30 Participants

Primary: Renal Video Intensity Units — 19 units on a scale

Primary: Number of Participants Experiencing Urinary Tract Infection Within 6 Weeks of Surgery — 13; 13 Participants — p=0.97

Primary: Need for Any Intermittent Catheterization Postoperatively as a Binary Outcome — 18; 22 Participants

Primary: Postoperative Urinary Retention — 16; 5 Participants

Primary: The Number of Participants Who Completed and Discontinued the Study — 11; 10; 1; 1 Participants — p=0.949

Primary: Residual Urine Measured by Ultra Sound — 11; 6 ml — p=0.56

Primary: Number of Participants With Postoperative Urinary Retention — 11; 11 Participants — p=0.5

Primary: Urine Output of SOC Device Versus Accuryn — 0; 5 Patients with airlocks

Primary: Incidence of Bladder Irritation Symptoms (e.g. Frequency, Urgency, Nocturia, Urine Leakage...) Associated With the RELIEF Stent. — 51.95 Units on a scale

Primary: Number of Participants With Acute Urinary Retention — 6; 7 Participants

Primary: Number of Participants With Urinary Retention — 0; 11; 74; 63 Participants

Primary: Bladder Scan Measurements of Residual Urine Volume — 32.74; 34.78 Residual volume in mL — p=0.8762

Primary: Participants With Urine Cultures With Bacteriuria (>100,000 Cfu/ml or >=100,000 Cfu/ml) Plus Pyuria (Any WBC) — 26; 32; 21; 27 participants

Primary: Ureteral Stent Symptom Questionnaire Score Up to 24 Hours Prior to Stent Insertion — 1.76; 1.84; 2.02; 1.93 score on a scale

Primary: Number of Subjects Catheterized Within the Six-week Post-operative Period Following Surgical Repair of Prolapse, Among Those Discharged Without a Urinary Catheter. — 2…

Primary: Successful Trial Without Catheter Peri-procedurally — 29; 0 Participants

Primary: Persistent Retention — 29; 21 participants

Primary: The Incidence of UTI — 66; 54 Participants — p=0.299

Primary: Change in Urge Incontinence Episodes — 3.9 UUI

Primary: Number of Participants Who Achieved Post-void Residual (PVR) of ≤150 ml Over 90 Days — 79 Participants

Primary: Incidence of Urinary Track Infection (UTI) — 62; 71 Participants

Primary: Change in Nocturnal Polyuria Index — 41.7; 41.7; 34.5; 37.8 percentage of urine volume — p=0.3