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NCT03364127 · ClinicalTrials.gov registry record · NA

Effect of Acupuncture on Patient Vulvodynia Outcomes

A NA study, sponsored by University of Illinois at Chicago.

Completed
Registry status
NA
Development phase
89
Enrollment target

NCT03364127 is a NA study that has completed, run by University of Illinois at Chicago. The registered enrollment target is 89 participants.

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The verdict

NCT03364127, a NA study, has completed, sponsored by University of Illinois at Chicago.

COMPLETED
Registry status
NA
Development phase
89 participants
Enrollment target

Study Summary

This study evaluates acupuncture for the treatment of vulvodynia; specifically if it reduces vulvar pain and pain with intercourse. It also examines how long the effect of acupuncture lasts in women with vulvodynia. Half of the women will receive acupuncture and the other half will receive placebo acupuncture. Women who get a reduction in pain will monitor there pain once a week for up to 12 weeks to see how long the acupuncture effect lasts.

Interventions

  • OTHER Active Acupuncture
  • OTHER Placebo Acupuncture

Trial Details

FieldValue
Enrollment Target 89 participants
Start Date 2018-02-23
Est. Completion 2022-11-07
Phase NA

Sponsor

University of Illinois at Chicago

430 total trials

What the Registry Record Tells You About NCT03364127

The ClinicalTrials.gov registry entry for NCT03364127 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 89 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Illinois at Chicago, which has 430 total studies on file at ClinicalTrials.gov.

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

NCT03364127 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03364127 about?

NCT03364127 is a clinical study titled "Effect of Acupuncture on Patient Vulvodynia Outcomes". This study evaluates acupuncture for the treatment of vulvodynia; specifically if it reduces vulvar pain and pain with intercourse. It also examines how long the effect of acupuncture lasts in women with vulvodynia. Half of the women will receive acupuncture and the other half will receive placebo a...

What is the current status of trial NCT03364127?

This trial is currently completed. It is a NA study. The enrollment target is 89 participants. The study started on 2018-02-23. Estimated completion is 2022-11-07.

What interventions are being tested in trial NCT03364127?

The interventions under investigation include: Active Acupuncture (OTHER), Placebo Acupuncture (OTHER).

Who is sponsoring clinical trial NCT03364127?

This trial is sponsored by University of Illinois at Chicago, which has 430 total clinical trials registered on ClinicalTrials.gov.

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.