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Voiding Protocols After Minimally Invasive Hysterectomy

N/A

Recruiting

Led By Kristin Patzkowsky

Research Sponsored by Johns Hopkins University

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Women 18+ undergoing minimally invasive benign, non-urogynecologic hysterectomy

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 2 years

Awards & highlights

Study Summary

This trialwill see if strict vs. liberal voiding affects post-op outcomes for patients discharged same-day after minimally invasive hysterectomy.

Who is the study for?

This trial is for women over 18 who speak English and are having a minimally invasive hysterectomy that isn't related to urology. They must be able to go home the same day of surgery. Women with past bladder surgeries, known urinary diseases, or those not leaving the hospital on the same day can't join.Check my eligibility

What is being tested?

The study is testing if it's necessary for patients to empty their bladders before going home after a non-urogynecologic hysterectomy. Participants will be randomly assigned either to a group that must void (pee) before discharge or one without this requirement.See study design

What are the potential side effects?

While there aren't direct side effects from voiding trials themselves, potential risks include increased chances of urinary retention (difficulty peeing), UTI, needing to return to the hospital, and possibly longer stays in recovery.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Select...

I am a woman over 18 having a minor surgery to remove my uterus for non-cancer reasons.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 2 years

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~2 years

This trial's timeline: 3 weeks for screening, Varies for treatment, and 2 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Rates of UTI

Rates of re-presentation to the ER

Rates of urinary retention

Secondary outcome measures

Amount of time spent in PACU

Cost of stay in PACU

Trial Design

2Treatment groups

Experimental Treatment

Placebo Group

Group I: No strict need to void following surgery before dischargeExperimental Treatment1 Intervention

Participants randomized to this arm will have no strict need to void following surgery before they are discharged.

Group II: Strict need to void following surgery before dischargePlacebo Group1 Intervention

Participants randomized to this arm will have a strict need to void following surgery before they are discharged.

0 / 1Eligibility criteria met

Find a Location

Who is running the clinical trial?

Johns Hopkins UniversityLead Sponsor

2,259 Previous Clinical Trials

14,820,553 Total Patients Enrolled

1 Trials studying Urinary Retention

154 Patients Enrolled for Urinary Retention

Kristin PatzkowskyPrincipal InvestigatorJohns Hopkins University

Krisitn PatzkowskyPrincipal InvestigatorJohns Hopkins University

Media Library

No Strict need to void following surgery Clinical Trial Eligibility Overview. Trial Name: NCT05108506 — N/A

Urinary Retention Research Study Groups: Strict need to void following surgery before discharge, No strict need to void following surgery before discharge

Urinary Retention Clinical Trial 2023: No Strict need to void following surgery Highlights & Side Effects. Trial Name: NCT05108506 — N/A

No Strict need to void following surgery 2023 Treatment Timeline for Medical Study. Trial Name: NCT05108506 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the participant count of this clinical investigation?

"Indeed, the details outlined on clinicaltrials.gov affirm that this medical trial is seeking participants. This research was originally announced December 5th 2022 and has since been updated on December 12th 2022. The study requires 100 individuals spread across 1 centre to take part in it."

Answered by AI

Are there still opportunities for participation in this medical experiment?

"Affirmative. According to information on clinicaltrials.gov, the trial that was initially launched on December 5th 2022 is now recruiting participants. 100 patients must be enrolled across a single site in order for this study to move forward successfully."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

Strict Need to Void After Same-day Discharge, Non-urogynecologic, Minimally Invasive Hysterectomy

2022. "Strict Need to Void After Same-day Discharge, Non-urogynecologic, Minimally Invasive Hysterectomy". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05108506.

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