NCT07893119

Brief Summary

Postpartum urinary retention is a common complication after childbirth, with a higher risk for women who undergo vaginal delivery with epidural analgesia. This study aims to determine whether performing the first void after the removal of an indwelling urinary catheter in a standing position in the shower, compared to sitting on a toilet, helps reduce postpartum urinary retention. The study will include 100 women who had a vaginal delivery with epidural analgesia. Participants will be randomly assigned to either void while standing in the shower (Group A) or sitting on the toilet (Group B). Immediately after this first spontaneous void, the post-void residual urine volume (PVR) will be measured using an ultrasound bladder scan. The study seeks to find out if the standing position facilitates more complete bladder emptying, reduces the need for recatheterization, and decreases perineal pain compared to the sitting position.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
38mo left

Started Oct 2026

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 19, 2026

Completed
1 day until next milestone

Study Start

First participant enrolled

October 20, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 23, 2026

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2029

Expected
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2029

Last Updated

October 23, 2026

Status Verified

July 1, 2026

Enrollment Period

2.8 years

First QC Date

October 19, 2026

Last Update Submit

October 19, 2026

Conditions

Keywords

Postpartum Urinary RetentionVaginal DeliveryEpidural AnalgesiaPost-Void Residual VolumeUrinary Catheter

Outcome Measures

Primary Outcomes (1)

  • Number of participants with Post-Void Residual Volume (PVR) > 150 mL

    Post-void residual urine volume (PVR) greater than 150 mL, measured by bladder ultrasound (bladder scan) immediately after the first spontaneous void following catheter removal. This cut-off is consistent with definitions of covert postpartum urinary retention.

    Immediately after the first void (within a maximum of 6 hours following catheter removal)

Secondary Outcomes (7)

  • Mean Post-Void Residual Volume (PVR)

    Immediately after the first void (within a maximum of 6 hours following catheter removal)

  • Incidence of Overt Postpartum Urinary Retention (PUR)

    Up to 6 hours after catheter removal

  • Need for Recatheterization

    Within 24-48 hours postpartum

  • Time to First Void

    Up to 6 hours after catheter removal

  • Incidence of Urinary Tract Infection (UTI)

    Within 7 days postpartum

  • +2 more secondary outcomes

Study Arms (2)

Group A - Standing Position

EXPERIMENTAL

Participants will perform their first void after catheter removal in a standing position in the shower.

Behavioral: Standing in the shower

Group B - Sitting Position

ACTIVE COMPARATOR

Participants will perform their first void after catheter removal in a sitting position on the toilet.

Behavioral: Sitting on the toilet

Interventions

The woman is assisted to the shower area and instructed to void in a standing position under running warm water.

Group A - Standing Position

he woman is assisted to the toilet and instructed to void in a sitting position.

Group B - Sitting Position

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsEligibility is restricted to individuals who have undergone a vaginal delivery
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

ssuta Ashdod Hospital

Ashdod, Israel

Location

Related Publications (3)

  • Ellahi A, Stewart F, Kidd EA, Griffiths R, Fernandez R, Omar MI. Strategies for the removal of short-term indwelling urethral catheters in adults. Cochrane Database Syst Rev. 2021 Jun 29;6(6):CD004011. doi: 10.1002/14651858.CD004011.pub4.

    PMID: 34184246BACKGROUND
  • Chou EC, Chang CH, Chen CC, Wu HC, Wu PL, Chen KL. Women urinate in the standing position do not increase post-void residual urine volumes. Neurourol Urodyn. 2010 Sep;29(7):1299-300. doi: 10.1002/nau.20868.

    PMID: 20878999BACKGROUND
  • Yang KN, Chen SC, Chen SY, Chang CH, Wu HC, Chou EC. Female voiding postures and their effects on micturition. Int Urogynecol J. 2010 Nov;21(11):1371-6. doi: 10.1007/s00192-010-1204-3. Epub 2010 Jul 1.

    PMID: 20593163BACKGROUND

MeSH Terms

Interventions

Standing Position

Intervention Hierarchy (Ancestors)

PostureMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Central Study Contacts

Elad Preuss, M.D

CONTACT

Amit Markovich, M.D

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Masking Details
Due to the obvious nature of the physical intervention (voiding position), participants and the staff assisting with voiding cannot be blinded. Masking is strictly applied to the healthcare professionals performing and recording the post-void residual (PVR) ultrasound measurements (outcomes assessors), as well as the investigators performing the data analysis.
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Participants will be randomized in a 1:1 ratio using a computer-generated sequence to one of two parallel groups just prior to the removal of their indwelling urinary catheter.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 19, 2026

First Posted

October 23, 2026

Study Start

October 20, 2026

Primary Completion (Estimated)

August 1, 2029

Study Completion (Estimated)

December 1, 2029

Last Updated

October 23, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will not share

Data sharing with other researchers is not planned as it was not included in the IRB-approved protocol and informed consent.")

Locations