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Needle therapy tested for painful sex condition

NCT ID NCT07534345

Symptom relief Sponsor: Université de Sherbrooke Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether dry needling—inserting fine needles into muscles—can reduce pain during intercourse for women with provoked vestibulodynia, a common cause of sharp vaginal pain. 170 women will receive either real or sham dry needling over 8 weekly sessions. The goal is to see if this low-risk treatment can offer relief where other options are limited.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
dry needling
What this could lead to
If it works, this could offer a low-risk, non-drug treatment option for women with painful intercourse due to provoked vestibulodynia.
What could go wrong
This is a mid-sized trial, but it's still early. The sham needle group may also show improvement, and results may not apply to all women with vulvar pain.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 170 people

The number the study aims to enrol. It can still change while the study runs.

Started

May 2026

Expected to finish

Jun 2029

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 45 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Women reporting vulvo-vaginal pain during intercourse for \>3 months with an average pain intensity of ≥5/10 on a numerical rating scale (NRS); * Confirmed diagnosis of provoked vestibulodynia by a gynecologist of our team following a standardized gynaecologic exam. Exclusion Criteria: * Other urogynecological and vulvar pain conditions (e.g., unprovoked pain, deep dyspareunia, dermatological condition); * Prior vulvovaginal or pelvic surgery; * Current pregnancy; * Postmenopausal status; * Having previously received DN or acupuncture; * Expected changes of medication that could influence pain perception (e.g., antidepressant); * Any significant coexisting medical conditions likely to interfere with the study procedures.

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Conditions

The condition(s) this trial relates to.

vulvodynia

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Provoked vestibulodynia

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    4 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Centre hospitalier universitaire de Québec - Université Laval

    NOT_YET_RECRUITING

    Québec, Quebec, G1V 4G2, Canada

  • Centre hospitalier universitaire de Sherbrooke

    RECRUITING

    Sherbrooke, Quebec, J1H 5N4, Canada

  • Cigonia

    RECRUITING

    Sherbrooke, Quebec, J1L 1C6, Canada

  • Kinatex l'Ormière

    NOT_YET_RECRUITING

    Québec, Quebec, G2B 3K3, Canada

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