Clinical trials: Urinary Retention After Procedure
Urinary Retention After Procedure
Donepezil Prevents Urinary Retention After Extensive Total Hysterectomy
Patients were randomly divided into experimental group and control group. The control group received routine postoperative treatment, while the experimental group took donepezil 5mg orally before going to bed every night from the…
- Trial name
- NCT05540977
- Testing
- Donepezil, Usual care
- Where
- China
- Volunteers
- 108 people
- Sponsor
- Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Stress Urinary Incontinence, Urinary Retention Postoperative
Incidence of Short-term Urinary Retention After Fascial Retropubic Sling: Prospective and Randomized Analysis.
The aim of this study is to evaluate the incidence of short-term urinary retention and the cure rate in patients with stress urinary incontinence undergoing surgical treatment with fascial pubovaginal sling with two tension…
- Conditions
- Stress Urinary Incontinence, Urinary Retention Postoperative, Urinary Retention After Procedure
- Trial name
- NCT04465578
- Testing
- Sling tension adjustment by classic technique, Sling tension adjustment by height of 4 cm
- Where
- Brazil
- Volunteers
- 56 people
- Sponsor
- Hospital de Clinicas de Porto Alegre
Urinary Retention
The Effect of Modified Supine Position on Urinary Elimination After Percutaneous Coronary Intervention
Urinary retention is also a frequent complication after percutaneous coronary intervention applied via the femoral artery. The inability to manage this situation effectively leads to serious complications in the long term…
- Trial name
- NCT06070545
- Testing
- Modified Supine Position
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Istanbul University - Cerrahpasa
Minimally Invasive Surgical Procedure, Hysterectomy
The Impact of Post-operative Voiding Trial on Length of Stay Following Laparoscopic Hysterectomy: A Prospective, Randomized Control Trial
The aim of this study is to investigate the impact of an active voiding trial compared to a passive voiding trial on time to discharge following a planned same day discharge laparoscopic hysterectomy.
- Conditions
- Minimally Invasive Surgical Procedure, Hysterectomy, Urinary Retention
- Trial name
- NCT04487600
- Testing
- Active voiding trial
- Volunteers
- 130 people, healthy volunteers welcome
- Sponsor
- Brigham and Women's Hospital
Catheter-Associated Urinary Tract Infection
Nitrofurantoin Administration for the Prevention of Short-Term Catheter Associated Urinary Tract Infection After Pelvic Surgery
The specific aim of this randomized double-blind placebo-controlled trial is to evaluate the efficacy of administration of nitrofurantoin prophylaxis after catheter discontinuation for the prevention of catheter-associated…
- Trial name
- NAUTICA (NCT03287089)
- Testing
- Nitrofurantoin 100 MG
- Where
- United States
- Volunteers
- 164 people
- Sponsor
- Wake Forest University Health Sciences
Urinary Retention, Urinary Retention After Procedure
Rectus Abdominis Detrusor Myoplasty for Urinary Retention
This investigates the outcomes of a surgical technique using the patient's own abdominal wall muscles to help contract the bladder in patients with urinary retention
- Conditions
- Urinary Retention, Urinary Retention After Procedure, Urinary Retention Postoperative
- Trial name
- RADM (NCT07379814)
- Testing
- Rectus Abdominal Detrusor Myoplasty
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- University Hospitals Cleveland Medical Center
Urinary Retention
Post Operative Urinary Retention (POUR) Following Thoracic Oncological Surgery
This is a feasibility study looking at whether the use of Tamsulosin could lower the high incidence of postoperative urinary retention (POUR) in older men who undergo an oncological thoracic surgical procedure for suspected or…
- Trial name
- NCT05657990
- Testing
- Tamsulosin
- Where
- 4 sites in United States
- Volunteers
- 46 people
- Sponsor
- Hackensack Meridian Health
Neuromuscular Blocking Agents, Urinary Retention After Procedure
NMBA Reversal and Postoperative Urinary Retention
In this single-center retrospective cohort study of adult patients who underwent surgery under general anesthesia at Beth Israel Deaconess Medical Center between September 2016 and January 2024, the association between the choice…
- Conditions
- Neuromuscular Blocking Agents, Urinary Retention After Procedure, Urinary Retention Postoperative, Neuromuscular Blockade Reversal Agent
- Trial name
- NCT06948409
- Testing
- Choice of reversal agent (sugammadex or neostigmine [with muscaranic antagonist])
- Where
- United States
- Volunteers
- 70,000 people, healthy volunteers welcome
- Sponsor
- Beth Israel Deaconess Medical Center