Urinary Retention After Vaginal Delivery With Epidural Anesthesia.

Status Recruiting

Clinical Trial Summary

The investigators intend to compare the rate of urinary retention among female patients after vaginal delivery under epidural anesthesia, depending on bladder catheterization type, either by a foley catheter inserted adjacent to epidural anesthesia or intermittent catheterization applied every 4 hours during labor.

Clinical Trial Description

An explanation about the study will be delivered to each participant and each participant will sign a confirmed consent. Patients will be randomized between 2 groups of treatment: 1. intermittent catheterization applied every 4 hours during labor. 2. foley catheter inserted adjacent to epidural anesthesia. In patients with a foley catheter, the catheter will be removed soon after delivery. Participants will be followed by a clinician post labor. An abdominal US will be performed either 4 hours after delivery or after the participant urinates to check the bladder volume. Patient information including demographic information, information regarding the patient's pregnancy and delivery will be collected from the patient's electronic record. ;

Study Design

Related Conditions & MeSH terms

Urinary Retention

Clinical Trial Details

NCT number	NCT02865551
Study type	Interventional
Source	Rambam Health Care Campus
Contact	Roy Lauterbach, MD
Phone	972529432416
Email	r_lauterbach@rambam.health.gov.il
Status	Recruiting
Phase	N/A
Start date	July 1, 2019
Completion date	December 31, 2023

View Details

See also
Status	Clinical Trial	Phase
Withdrawn	`NCT05538273` - Optimal Management of Urinary Catheter in Gyn Onc
Recruiting	`NCT05065255` - Study of the Criteria for Choosing Speedicath Catheters During the Initiation of Self-catheterization
Completed	`NCT04236596` - Pudendal Nerve Mapping Towards Improved Neuromodulation for Urinary Retention	N/A
Completed	`NCT05526651` - Improvement of Urinary Retention Symptoms With Electroacupuncture Therapy	N/A
Not yet recruiting	`NCT06070545` - The Effect of Modified Supine Position on Urinary Elimination After Percutaneous Coronary Intervention	N/A
Recruiting	`NCT03314025` - Prophylactic Tamsulosin in Prevention of Post-operative Urinary Retention in Men After Transanal Endoscopic Microsurgery	Phase 2
Recruiting	`NCT05439902` - Efficacy of Alpha-blockers (Tamsulosin) in the Treatment of Symptomatic Dysuria in Multiple Sclerosis in Women	N/A
Enrolling by invitation	`NCT05259800` - Peppermint Oil for Urinary Retention	N/A
Recruiting	`NCT06417346` - Comparison of Laparoscopic and Open Inguinal Hernia Repair in Elderly Patients	N/A
Completed	`NCT03296280` - Evaluation of Implementation of a National Point-of-Care Ultrasound Training Program
Completed	`NCT04715971` - Urinary Retention on an Acute Geriatric Hospitalisation Unit.
Completed	`NCT03302936` - Assessing Pyridium for Post-Sling Urinary Retention	Phase 4
Completed	`NCT02886143` - Effect of Active vs. Passive Voiding Trials on Time to Discharge, Urinary Tract Infection, and Urinary Retention	Phase 3
Completed	`NCT02749188` - Evaluation of Bladder Stimulation as a Noninvasive Technique of Urine Collection in Infant Who Have Not Acquired Walking	N/A
Completed	`NCT01220362` - Effects of Thoracic Epidural Analgesia and Surgery on Lower Urinary Tract Function: A Randomized, Controlled Study	N/A
Completed	`NCT01284361` - Comparison of Two Intermittent Urinary Catheters	N/A
Terminated	`NCT00804557` - Efficacy And Safety Of The Uro-Ease® Urinary Catheter During Clean Intermittent Catheterization	N/A
Terminated	`NCT00563485` - Randomized Trial Comparing Terazosin 5 mg Daily and Doxazosin GITS 4 mg Daily for Trial Without Catheter in Acute Urinary Retention With Long Term Follow up	N/A
Terminated	`NCT00563654` - Randomized Trial Comparing Alfuzosin GITS 10 mg Daily With Placebo for Trial Without Catheter in Acute Urinary Retention With Long Term Follow up	N/A
Terminated	`NCT04682366` - The Effect of Tamsulosin on Postoperative Urinary Retention	Phase 4