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NCT06366269 · ClinicalTrials.gov registry record · NA

Acupuncture First for IC/BPS

A NA study of Interstitial Cystitis and Bladder Pain Syndrome, sponsored by University Hospitals Cleveland Medical Center.

Recruiting
Registry status
NA
Development phase
34
Enrollment target
1
Study location

NCT06366269 is a NA study of Interstitial Cystitis and Bladder Pain Syndrome that is actively recruiting participants, run by University Hospitals Cleveland Medical Center. The registered enrollment target is 34 participants, below the 361-participant average among 26 other Interstitial Cystitis trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06366269, a NA study of Interstitial Cystitis and Bladder Pain Syndrome, is actively recruiting participants, sponsored by University Hospitals Cleveland Medical Center.

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

Study Summary

The goal of this clinical trial is to learn if acupuncture in addition to behavioral changes can better treat in women with bladder pain syndrome (also known as interstitial cystitis) that have not received other treatments. The main question it aims to answer is: Does acupuncture improve pain symptoms on the Interstitial Cystitis Index? Researchers will compare six (6) weeks behavioral management alone to behavioral management and acupuncture. Participants will * complete surveys about their bladder pain symptoms * make behavioral changes that have been shown to improve bladder pain symptoms * attend six (6) weekly acupuncture sessions * attend six (6) weekly physical therapy sessions after finishing acupuncture

Interventions

  • OTHER Acupuncture
  • OTHER Physical therapy
  • BEHAVIORAL Behavioral management

Study Locations (1)

Ohio

  • University Hospitals - Cleveland

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2025-01-21
Est. Completion 2026-10
Phase NA

What the Registry Record Tells You About NCT06366269

The ClinicalTrials.gov registry entry for NCT06366269 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 34 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 361-participant average among 26 other Interstitial Cystitis trials with a reported enrollment target (91% lower). The listed sponsor is University Hospitals Cleveland Medical Center, which has 230 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Interstitial Cystitis appearing as the primary indexed condition, and to 3 interventions - of which Acupuncture is the first listed.

NCT06366269 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT06366269 about?

NCT06366269 is a clinical study titled "Acupuncture First for IC/BPS". The goal of this clinical trial is to learn if acupuncture in addition to behavioral changes can better treat in women with bladder pain syndrome (also known as interstitial cystitis) that have not received other treatments. The main question it aims to answer is: Does acupuncture improve pain symp...

What is the current status of trial NCT06366269?

This trial is currently recruiting. It is a NA study. The enrollment target is 34 participants. The study started on 2025-01-21. Estimated completion is 2026-10.

What conditions does trial NCT06366269 study?

This clinical trial studies the following conditions: Interstitial Cystitis, Bladder Pain Syndrome.

What interventions are being tested in trial NCT06366269?

The interventions under investigation include: Acupuncture (OTHER), Physical therapy (OTHER), Behavioral management (BEHAVIORAL).

Who is sponsoring clinical trial NCT06366269?

This trial is sponsored by University Hospitals Cleveland Medical Center, which has 230 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06366269 being conducted?

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

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