Clinical Trials Directory

Trials / Terminated

TerminatedNCT05259800

Peppermint Oil for Urinary Retention

Evaluating the Use of Peppermint Oil for Postpartum Women With Urinary Retention

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
17 (actual)
Sponsor
TriHealth Inc. · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
OTHERPeppermint oil vaporsSubjects will be exposed to vapor of peppermint oil
OTHERMineral OilSubjects will be exposed to vapor of placebo (mineral oil)

Timeline

Start date
2021-10-05
Primary completion
2025-04-01
Completion
2025-04-01
First posted
2022-03-02
Last updated
2025-08-29
Results posted
2025-08-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05259800. Inclusion in this directory is not an endorsement.