Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00297427 · ClinicalTrials.gov registry record · Phase 2

Acupuncture for Urinary Incontinence

A Phase 2 study, sponsored by University of Pittsburgh.

Completed
Registry status
Phase 2
Development phase
127
Enrollment target

NCT00297427: Completed Phase 2 study, sponsored by University of Pittsburgh.

NCT00297427 is a Phase 2 study that has completed, run by University of Pittsburgh. The registered enrollment target is 127 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00297427, a Phase 2 study, has completed, sponsored by University of Pittsburgh.

COMPLETED
Registry status
Phase 2
Development phase
127 participants
Enrollment target

Study Summary

This research study will evaluate the effectiveness of acupuncture in decreasing urinary incontinence (involuntary urine loss) in women. The study will involve 12 acupuncture sessions over 6 weeks. We will compare the effectiveness of acupuncture and sham (placebo) acupuncture (a procedure in which the needle feels like it penetrates the skin, but is not actually inserted into the body) on the frequency and volume of involuntary (accidental) urine loss after completing the intervention, and again one month later. Individuals participating in this study will be randomly assigned to receive either the actual or sham acupuncture. Randomization means being assigned by chance, similar to flipping a coin. Study participants will not know which group (actual or sham acupuncture) they were assigned to until one month after completing the 6-weeks of treatment. The sham acupuncture needles look similar to the real acupuncture needles and feel like they penetrate the skin, but do not actually do so. If individuals are assigned to the sham acupuncture group, they will be eligible to receive the actual acupuncture one month after completing the sham acupuncture if they wanted to. All individuals will be followed for 6 months after completing the acupuncture treatments.

Primary Outcome

Percent change in incontinent episodes (measured by self-report electronic bladder diary) at 1 week post-intervention (true or sham acupuncture) relative to baseline.

Interventions

  • PROCEDURE Acupuncture
  • OTHER Sham acupuncture

Trial Details

FieldValue
Enrollment Target 127 participants
Start Date 2005-10
Est. Completion 2011-07
Phase Phase 2
University of Pittsburgh

1,238 total trials

What the finished NCT00297427 record still lists

NCT00297427 is an interventional study that assigns participants to a tested intervention. The registered 127 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which Acupuncture is the first listed.

NCT00297427 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00297427 about?

NCT00297427 is a clinical study titled "Acupuncture for Urinary Incontinence". This research study will evaluate the effectiveness of acupuncture in decreasing urinary incontinence (involuntary urine loss) in women. The study will involve 12 acupuncture sessions over 6 weeks. We will compare the effectiveness of acupuncture and sham (placebo) acupuncture (a procedure in which ...

What is the current status of trial NCT00297427?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 127 participants. The study started on 2005-10. Estimated completion is 2011-07.

What interventions are being tested in trial NCT00297427?

The interventions under investigation include: Acupuncture (PROCEDURE), Sham acupuncture (OTHER).

Who is sponsoring clinical trial NCT00297427?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00297427's enrollment target sits among peer trials

127 555th of 2000 higher than 1,445 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03017820 · 127 participants · Phase 1

    A Vaccine (VSV-hIFNβ-NIS) With or Without Cyclophosphamide and Combinations of Ipilimumab, Nivolumab, and Cemiplimab in Treating Relapsed or Refractory Multiple Myeloma, Acute Myeloid Leukemia or Lymphoma

  • NCT03609580 · 127 participants · Phase 1

    Post-operative Urinary Retention (POUR) Following Thoracic Surgery

  • NCT06285643 · 127 participants · Phase 2

    A Study of AAV2-GDNF in Adults With Moderate Parkinson's Disease (REGENERATE-PD)

  • NCT06809400 · 127 participants · Phase 1

    A Study of LY4006896 in Healthy Participants and Participants With Parkinson's Disease

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00297427, the US trial registry maintained by the National Library of Medicine. NCT00297427 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.