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

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