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NCT06369922 · ClinicalTrials.gov registry record · NA

TENS Analgesia During Outpatient Urethral Bulking for Stress Urinary Incontinence.

A NA study of Pain and Urinary Incontinence, sponsored by University of Rochester.

Recruiting
Registry status
NA
Development phase
100
Enrollment target
1
Study location

NCT06369922 is a NA study of Pain and Urinary Incontinence that is actively recruiting participants, run by University of Rochester. The registered enrollment target is 100 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (67% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06369922, a NA study of Pain and Urinary Incontinence, is actively recruiting participants, sponsored by University of Rochester.

RECRUITING
Registry status
NA
Development phase
100 participants
Enrollment target
1
Study location

Study Summary

This will be a double-blind randomized control trial in women with stress urinary incontinence who are undergoing an outpatient transurethral bulking procedure for stress urinary incontinence. Subjects will be identified by the University of Rochester urologists and urogynecologists participating in the study who currently oversee stress incontinence care. Subjects will be randomized into two groups. One group will be undergoing the cystoscopy with transcutaneous electrical nerve stimulation (TENS) for analgesia, and the second group will have the cystoscopy with placebo TENS.

Interventions

  • PROCEDURE TENS
  • PROCEDURE Control TENS

Study Locations (1)

New York

  • Pelvic Health and Continence Specialties - Rochester

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2024-07-01
Est. Completion 2026-06-01
Phase NA

Sponsor

University of Rochester

636 total trials

What the Registry Record Tells You About NCT06369922

The ClinicalTrials.gov registry entry for NCT06369922 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 304-participant average among 374 other Pain trials with a reported enrollment target (67% lower). The listed sponsor is University of Rochester, which has 636 total studies on file at ClinicalTrials.gov.

The record links to 5 conditions, with Pain appearing as the primary indexed condition, and to 2 interventions - of which TENS is the first listed.

NCT06369922 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT06369922 about?

NCT06369922 is a clinical study titled "TENS Analgesia During Outpatient Urethral Bulking for Stress Urinary Incontinence.". This will be a double-blind randomized control trial in women with stress urinary incontinence who are undergoing an outpatient transurethral bulking procedure for stress urinary incontinence. Subjects will be identified by the University of Rochester urologists and urogynecologists participating in...

What is the current status of trial NCT06369922?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2024-07-01. Estimated completion is 2026-06-01.

What conditions does trial NCT06369922 study?

This clinical trial studies the following conditions: Pain, Urinary Incontinence, Pain, Acute, Urinary Incontinence,Stress, Stress Incontinence Female.

What interventions are being tested in trial NCT06369922?

The interventions under investigation include: TENS (PROCEDURE), Control TENS (PROCEDURE).

Who is sponsoring clinical trial NCT06369922?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06369922 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.