Clinical trials: Post Operative Urinary Retention
Urinary Retention Postoperative
Strict Need to Void After Same-day Discharge, Non-urogynecologic, Minimally Invasive Hysterectomy
Patients who are undergoing non-urogynecologic, minimally invasive (laparoscopic, robotic) hysterectomy who are discharged the day of surgery will be randomized to a strict need to void versus no need to void prior to discharge.
- Trial name
- NCT05108506
- Testing
- No Strict need to void following surgery, Strict need to void following surgery
- Where
- United States
- Volunteers
- 205 people, healthy volunteers welcome
- Sponsor
- Johns Hopkins University
Urinary Retention, Postoperative Complications
Post-Operative Voiding After Gynecological Surgery Trial
To determine whether partially filling the bladder after outpatient gynaecological laparoscopy expedites time to first void and discharge.
- Conditions
- Urinary Retention, Postoperative Complications, Surgery
- Trial name
- POVAGS (NCT04198285)
- Testing
- Retrograde bladder filling
- Where
- Canada
- Volunteers
- 42 people, healthy volunteers welcome
- Sponsor
- Women's College Hospital
Urinary Retention
Preoperative Tamsulosin to Prevent Postoperative Urinary Retention After Surgery For Pelvic Floor Disorders
Our hypothesis is that patients receiving preoperative Tamsulosin will have decrease rates of postoperative urinary retention (POUR) after surgery in females for pelvic floor disorders.
- Trial name
- NCT04232683
- Testing
- Tamsulosin 0.4Mg Capsule
- Where
- United States
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- The Cleveland Clinic
Urinary Retention
Post-operative Urinary Retention (POUR) Following Thoracic Surgery
Inability to urinate a common complication that happens to many patients after a surgery, especially in men over 60 years of age who undergo surgery on their chest.
- Trial name
- POUR (NCT03609580)
- Testing
- Tamsulosin - 1 week, Tamsulosin - 3 days
- Where
- United States
- Volunteers
- 127 people, healthy volunteers welcome
- Sponsor
- Hackensack Meridian Health
Urinary Retention
Treatment for Acute Postoperative Voiding Dysfunction
If patients are unable to have their foley catheter removed because their bladder is not emptying well, they may be eligible for study participation.
- Trial name
- PTNS (NCT01189136)
- Testing
- PTNS Active Treatment
- Where
- United States
- Volunteers
- 84 people, healthy volunteers welcome
- Sponsor
- Women and Infants Hospital of Rhode Island
Post Operative Urinary Retention
Tamsulosin to Prevent Postoperative Urinary Retention in Laparoscopic Inguinal Hernia Repair
To investigate the effect of tamsulosin on the development of post-operative urinary retention (PUR) after elective laparoscopic inguinal hernia repair (LIHR).
- Trial name
- NCT04434378
- Testing
- Tamsulosin
- Where
- United States
- Volunteers
- 170 people, healthy volunteers welcome
- Sponsor
- Jewish Hospital, Cincinnati, Ohio
Urinary Retention, Anesthesia, Spinal
Postoperative Urinary Retention in Orthopedic Patients
The objective of this study is to compare the incidence of postoperative urinary retention related to spinal anesthesia with morphine and spinal anesthesia associated with peripheral blockade in orthopedic procedures of lower…
- Conditions
- Urinary Retention, Anesthesia, Spinal, Orthopedic Procedures, Nerve Block
- Trial name
- NCT04298775
- Testing
- spinal anesthesia with morphine, spinal anesthesia without morphine + peripheral nerve block
- Volunteers
- 52 people, healthy volunteers welcome
- Sponsor
- Hospital de Clinicas de Porto Alegre
Urinary Tract Infections, Urinary Retention
Can Investigators Reduce Urinary Catheter Use and Lower Urinary Tract Infection Among Women Undergoing Benign Gynecologic Surgery?
This is a randomized comparative trial investigating two different catheter management strategies among post-gynecologic surgery patients.
- Conditions
- Urinary Tract Infections, Urinary Retention, Satisfaction
- Trial name
- CAUTI (NCT03127280)
- Testing
- Fast Track foley removal
- Where
- United States
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- The Christ Hospital
Urinary Retention
Optimal Management of Urinary Catheter in Gyn Onc
This is a combined retrospective observational study that will collect data on urinary catheter removal of patients who underwent pelvic surgery by a gynecologic oncologist to assess timing safety and its implications in…
- Trial name
- NCT05538273
- Testing
- Early removal of urinary catheter postoperatively, Late removal of urinary catheter postoperatively
- Where
- United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- WellSpan Health
Postoperative Urinary Retention
Routine Bladder Catheterisation Through Fast-track Hip and Knee Replacement - What Are the Consequences?
To describe the need for re-catheterization and incidence of urological complications of routine use of perioperative fixed urinary catheter (KAD) for up to 24 hours of fast-track THA and TKA
- Trial name
- NCT02133768
- Where
- Denmark
- Volunteers
- 800 people, healthy volunteers welcome
- Sponsor
- Lundbeck Foundation
Urinary Retention, Lower Urinary Tract Symptoms
Tamsulosin vs Placebo to Prevent Postoperative Urinary Retention in Female Pelvic Reconstructive Surgery
This is a placebo controlled randomized controlled trial of perioperative use of tamsulosin to prevent postoperative urinary retention in female pelvic reconstructive surgery.
- Conditions
- Urinary Retention, Lower Urinary Tract Symptoms, Stress Urinary Incontinence, Pelvic Organ Prolapse
- Trial name
- NCT03524339
- Testing
- Tamsulosin
- Where
- 2 sites in United States
- Volunteers
- 132 people, healthy volunteers welcome
- Sponsor
- University Hospitals Cleveland Medical Center
Postoperative Retention of Urine, Postoperative Urinary Tract Infection
Day Zero Urinary Catheter Removal in Gen Thoracic Surgery Patients
Current standard of practice in study institution dictates day of surgery urinary catheter removal in general thoracic surgery patients receiving thoracic epidural analgesia.
- Trial name
- NCT01309529
- Where
- United States
- Volunteers
- 45 people, healthy volunteers welcome
- Sponsor
- Memorial Health System
Urinary Retention
Trial of Two Techniques to Assess Postoperative Voiding Function
Stress urinary incontinence (SUI) is a common condition that affects up to 35% of women. Many surgical procedures have been developed to treat SUI, and midurethral slings have gradually become the first line treatment.
- Trial name
- NCT02150083
- Testing
- OR retrograde fill
- Where
- United States
- Volunteers
- 59 people, healthy volunteers welcome
- Sponsor
- University of North Carolina, Chapel Hill
Postoperative Urinary Retention, Total Hip Arthroplasty
RCT Foley Catheter Study for Elective TJA
Urinary retention is a known complication following surgical procedures, with a theoretical increased risk in patients receiving neuraxial anesthesia due to a decreased ability to sense bladder distension.
- Conditions
- Postoperative Urinary Retention, Total Hip Arthroplasty, Total Knee Arthroplasty
- Trial name
- NCT05428020
- Testing
- Indwelling foley catheter, No foley catheter
- Where
- United States
- Volunteers
- 388 people, healthy volunteers welcome
- Sponsor
- Rush University Medical Center
Urinary Retention Postoperative, Laparoscopic Cholecystectomy
Postoperative Urinary Retention After Reversal of Neuromuscular Block by Neostigmine Versus Sugammadex
This study is intended to be a single-site, prospective, randomized, controlled study that intends to enroll a total of 230 patients undergoing laparoscopic cholecystectomy at Parkland Hospital.
- Conditions
- Urinary Retention Postoperative, Laparoscopic Cholecystectomy, Neuromuscular Blockade, Sugammadex
- Trial name
- NCT05794503
- Testing
- Neostigmine, Sugammadex
- Where
- United States
- Volunteers
- 235 people, healthy volunteers welcome
- Sponsor
- University of Texas Southwestern Medical Center
Urinary Retention Postoperative, Voiding Disorders
Optimization of Spontaneous Postoperative Trial of Void Among Women
Trial of void (TOV) is a diagnostic test performed on all women who undergo prolapse repair or incontinence surgery, due to the importance of diagnosing postoperative urinary retention (POUR).
- Trial name
- OPTION (NCT04010656)
- Testing
- PVR-based self-catheterization
- Where
- United States
- Volunteers
- 183 people, healthy volunteers welcome
- Sponsor
- Women and Infants Hospital of Rhode Island
Postoperative Voiding Dysfunction, Postoperative Urinary Retention
Void Trials After Two Voiding Trials (TVT)
The primary objective of this project is to compare the rate of postoperative voiding dysfunction in two voiding trials (the retrograde-fill technique versus the spontaneous-fill technique) after midurethral sling (MUS)…
- Trial name
- NCT03937531
- Testing
- Bladder Scanner
- Where
- 2 sites in United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- Icahn School of Medicine at Mount Sinai
Stress Urinary Incontinence
The Impact of Retropubic Lidocaine vs Saline on Postoperative Urinary Retention Following Midurethral Sling
Stress urinary incontinence affects millions of women worldwide and has a profound impact on the quality of life of older individuals, their subjective health status, levels of depression and need for care.
- Trial name
- NCT03913845
- Testing
- lidocaine with epinephrine, Normal saline with epinephrine
- Where
- 4 sites in United States
- Volunteers
- 150 people, healthy volunteers welcome
- Sponsor
- West Penn Allegheny Health System
Post-Op Complication
Comparison of Intrathecal Dexmedetomidine Versus Fentanyl as Adjuvants to Bupivacaine on Post-operative Urinary Retention in Knee Joint Arthroscopic Surgeries
The aim of this study was to assess the effect of intrathecally injected 5 µg dexmedetomidine or 25 µg fentanyl as adjuvants to bupivacaine in low dose spinal anesthesia for unilateral arthroscopic knee surgeries, on…
- Trial name
- NCT05596552
- Testing
- hyperbaric bupivacaine and dexmedetomidine, Bupivacaine-Fentanyl group
- Where
- Egypt
- Volunteers
- 70 people, healthy volunteers welcome
- Sponsor
- Ain Shams University
Urinary Retention Postoperative
At Home Early vs. Delayed Catheter Removal Following Failed Postoperative Voiding Trial: a Randomized Trial
This study aims to investigate whether patients who self-remove their indwelling transurethral catheters on POD 1 have similar rates of postoperative catheter reinsertion for urinary retention (within the first 7 days after…
- Trial name
- AHEADCARE (NCT05353400)
- Testing
- Early urinary catheter removal, Urinary catheter removal on POD 3
- Where
- United States
- Volunteers
- 9 people, healthy volunteers welcome
- Sponsor
- Wake Forest University Health Sciences