Peppermint Oil for Urinary Retention

Status Enrolling by invitation

Clinical Trial Summary

A randomized controlled study will be conducted, with two arms. Postpartum women experiencing urinary retention will be randomized into one of the two following arms: - Arm 1: Subjects will be exposed to vapor of peppermint oil - Arm 2: Subjects will be exposed to vapor of placebo (mineral oil) Outcome variables include resolution of urinary retention, time to spontaneous urination, volume of spontaneous urination, frequency of urinary catheterization, and patient satisfaction.

Clinical Trial Description

The purpose of the study is to determine if the use of peppermint oil among postpartum women experiencing urinary retention will increase spontaneous urination and decrease the need for catheterization. A randomized controlled study will be conducted, with two arms. Subjects will be randomized into one of the two following arms: - Arm 1: Subjects will be exposed to vapor of peppermint oil - Arm 2: Subjects will be exposed to vapor of placebo (mineral oil) Outcome variables include resolution of urinary retention, time to spontaneous urination, volume of spontaneous urination, frequency of urinary catheterization, and patient satisfaction. ;

Study Design

Related Conditions & MeSH terms

Urinary Retention

Clinical Trial Details

NCT number	NCT05259800
Study type	Interventional
Source	TriHealth Inc.
Contact
Status	Enrolling by invitation
Phase	N/A
Start date	October 5, 2021
Completion date	March 30, 2026

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Withdrawn	`NCT05538273` - Optimal Management of Urinary Catheter in Gyn Onc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
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	`NCT01284361` - Comparison of Two Intermittent Urinary Catheters	N/A
Completed	`NCT01220362` - Effects of Thoracic Epidural Analgesia and Surgery on Lower Urinary Tract Function: A Randomized, Controlled Study	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
Terminated	`NCT03843073` - Connected Catheter- Safety and Effectiveness Study	N/A