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Urinary Retention clinical trials

View clinical trials related to Urinary Retention.

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NCT ID: NCT04597372 Recruiting - Clinical trials for Urinary Retention Postoperative

Impact of Tamsulosin on Post-Operative Urinary Retention Following Pelvic Reconstructive Surgery

Start date: November 3, 2021
Phase: Phase 2
Study type: Interventional

The objective of the study is to determine the effectiveness of postoperative Tamsulosin in reducing the duration of acute postoperative urinary retention (POUR) following pelvic reconstructive surgery through a double blind, randomized placebo-controlled trial.

NCT ID: NCT04557787 Completed - Retention, Urinary Clinical Trials

Investigation of Non-CE Marked Intermittent Catheters for Females

Start date: December 1, 2020
Phase: N/A
Study type: Interventional

Investigation of novel non-CE marked intermittent catheters. The study was a randomized, single blinded, cross-over investigation comparing two new catheters for females with a comparator catheter.

NCT ID: NCT04555343 Completed - Prostate Cancer Clinical Trials

Intravesical Antifibrinolytic for Patients With Hematuria and Clot Retention

Start date: March 1, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

A study looking at the feasibility of doing a full-scale RCT that investigates the use of tranexamic acid intravesically prior to continuous bladder irrigation treatment in the emergency department for urinary retention due to clots. We want to know: - patient experience and acceptability of the intervention - study procedures (recruitment, site appropriateness, staff engagement) - safety data - identify resource use

NCT ID: NCT04543136 Completed - Retention, Urinary Clinical Trials

Investigation of Non-CE Marked Intermittent Catheters.

Start date: October 3, 2020
Phase: N/A
Study type: Interventional

Investigation of novel non-CE marked intermittent catheters. The study was a randomized, single blinded, cross-over investigation comparing two new catheters for males with a comparator catheter

NCT ID: NCT04535765 Completed - Hemorrhoids Clinical Trials

Effect of Early Warm Water Sitz Bath on Urinary Retention After Hemorrhoidectomy

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

Background: Hemorrhoid is one of the most common chronic anorectal diseases. The prevalence rate is about 44%. It occurs in adults aged 45-65 years. Hemorrhoidetomy resection is still the standard treatment for grade III and IV hemorrhoid. Urinary retention is one of the most common complications after hemorrhoid surgery, and the complications occur within 24 hours after surgery. The warm water sitz bath is a routine nursing care after hemorrhoid surgery in the clinic. The purpose is to provide moist heat of the perineum and anus to clean, promote healing and drainage, relieve pain, stimulate urination and promote relaxation. In contrast, all current studies, warm water sitz bath intervention time is the first day after surgery, the complications within 24 hours after surgery are not alleviated. Objective: The main purpose was to use experimental research methods to verify the effect of early warm water sitz bath on urinary retention after hemorrhoidectomy. The secondary objective was the effect of early warm water sitz bath on wound pain after hemorrhoidectomy. Methods: This study was a single-blind randomized trial in which subjects were randomly assigned to an experimental or control group with symptomatic stage III or IV end hemorrhoid who were admitted to the hospital for hemorrhoidectomy. The experimental group started the warm water bath 6 hours after the end of the operation, while the control group started the warm water sitz bath on the first day after the operation. The investigator assessed the amount of residual urine and wound pain index before and after each operation of the warm water sitz bath after surgery, and each subject was evaluated 8 times until 24 hours after surgery.

NCT ID: NCT04506866 Terminated - Overactive Bladder Clinical Trials

InterStim Micro Post Market Clinical Follow-up Study

ELITE
Start date: August 25, 2020
Phase: N/A
Study type: Interventional

Post-market clinical follow-up for continued assessment of safety and performance to confirm long-term outcomes of the InterStim Micro System for sacral neuromodulation.

NCT ID: NCT04491526 Recruiting - Inguinal Hernia Clinical Trials

Study to Prevent Postoperative Urinary Retention

STOP-POUR
Start date: November 1, 2020
Phase: Phase 4
Study type: Interventional

Post-operative urinary retention (POUR) is a common complication after inguinal hernia repair with a reported incidence up 34%. It can be described as the inability to initiate urination or properly empty one's bladder following surgery. It is usually self-limited, but it requires the use of catheterization to empty the bladder in order to prevent further injury to the bladder or kidneys and to relief the discomfort of a full bladder. Tamsulosin is a medication that is commonly used in men with urinary symptoms related to an enlarged prostate. There is some evidence to suggest that it may also potentially be beneficial for preventing post-operative urinary retention. The purpose of this study is to determine if tamsulosin ("TAMSULOSIN Mepha Ret Depocaps 0.4 mg") is effective in preventing post-operative urinary retention following endoscopic total extraperitoneal inguinal hernia repair and its impact on hospital length of stay.

NCT ID: NCT04487600 Completed - Urinary Retention Clinical Trials

The Impact of Post-operative Voiding Trial on Length of Stay Following Laparoscopic Hysterectomy: A Prospective, Randomized Control Trial

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

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. The investigators hypothesize that performing an active voiding trial will assess urinary function and lead to a reduction in length of stay.

NCT ID: NCT04473469 Completed - Urinary Retention Clinical Trials

Previously Implanted Pudendal Nerve Stimulation

Start date: January 19, 2021
Phase: N/A
Study type: Interventional

This study seeks to examine the response of the bladder to different pudendal nerve stimulation frequencies, by studying patients who have been previously-implanted with pudendal nerve neurostimulators.

NCT ID: NCT04465578 Recruiting - Clinical trials for Stress Urinary Incontinence

Incidence of Short-term Urinary Retention After Fascial Retropubic Sling: Prospective and Randomized Analysis.

Start date: February 10, 2020
Phase: N/A
Study type: Interventional

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 adjustment techniques: the classic adjustment technique ("2 fingers") and measuring the distance between the fixation knot and the aponeurosis of 4 cm.