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Urinary Retention clinical trials

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NCT ID: NCT05643950 Withdrawn - Urinary Retention Clinical Trials

Effectiveness and Cost-effectiveness of the T-Control® Catheter in Patients With Acute Urine Retention

Start date: August 1, 2023
Phase: N/A
Study type: Interventional

The general purpose of this study is to assess the preliminary effectiveness and cost-effectiveness of the T-Control® catheter versus the Foley type catheter in patients with Acute Urine Retention.

NCT ID: NCT05538273 Withdrawn - Urinary Retention Clinical Trials

Optimal Management of Urinary Catheter in Gyn Onc

Start date: September 8, 2022
Phase:
Study type: Observational

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 postoperative care.

NCT ID: NCT03937531 Withdrawn - Clinical trials for Postoperative Urinary Retention

Void Trials After Two Voiding Trials (TVT)

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

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) procedures with tension-free vaginal tape (TVT) without any concomitant surgery.

NCT ID: NCT02640326 Withdrawn - Clinical trials for Non-Small Cell Lung Cancer

McMaster Catheterization for Thoracoscopic Surgery Study

UCATh
Start date: December 1, 2018
Phase: N/A
Study type: Interventional

It is common practice to insert a Foley catheter into the bladder to drain urine during and after a lung resection. Recently, there has been increasing interest in the potential risks associated with this catheterization, particularly with regard to infection. As thoracic surgery adopts minimally invasive surgical techniques, the need for urinary catheterization during surgery is being questioned since these less invasive surgeries are known to result in less post-operative acute pain, shorter length of stay, and other outcomes that tend to decrease overall anesthetic needs for this patient population. Thus, there is a need to investigate whether patients who have had a minimally invasive lung resection truly need the Foley catheter at all. This will be achieved by assigning patients to either an experimental no-catheter group or the standard of care routine urinary catheter group to determine if patients with no catheter experience different rates of complications. This pilot study will primarily determine if there is a difference in post operative urinary complications between the groups. It is hoped that this study will definitively determine whether a Foley urine catheter is a necessary procedure in the course of a minimally invasive lung resection.

NCT ID: NCT01525498 Withdrawn - Clinical trials for Pelvic Organ Prolapse

Foley Catheterization Following Sacrocolpopexy

Start date: August 2011
Phase: N/A
Study type: Observational

The objective of this study is to prospectively evaluate the effects of early versus delayed removal of transuretheral catheters following sacrocolpopexy. The investigators specific aim is to determine the optimal time of removal of an indwelling transurethral catheter postoperatively in an effort to reduce the risk of postoperative urinary retention and urinary tract infection associated with catheter use. The investigators hypotheses are as follows: Hypothesis 1: Longer duration of postoperative catheter use will result in decreased postoperative urinary retention. Hypothesis 2: Shorter duration of postoperative catheter use will result in lower incidence of urinary tract infection.

NCT ID: NCT01305681 Withdrawn - Urinary Retention Clinical Trials

Bacterial Properties With LoFric® Catheters During Clean Intermittent Catheterization

Start date: May 6, 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objective of our study is to examine characteristics of bacteria that are discovered in urine from pediatric patients that utilize either LoFric® or non-LoFric® catheters for self intermittent catheterization. The investigators hypothesize that the hydrophilic nature of the LoFric® catheter will alter the microbial environment and reduce clinically significant urinary tract infections in patients with neurogenic bladder compared to a similar population using standard catheters. Secondary outcomes will be comparing the incidence of clinical urinary tract infections between patients that use standard catheters and those that use LoFric catheters. Lastly, patient satisfaction using LoFric catheters compared to standard catheters will be assessed.