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The Use of Acupuncture for the Treatment of Vulvar Vestibulitis

H

Hadassah Medical Center

Status

Completed

Conditions

Vestibulodynia

Treatments

Procedure: Acupuncture

Study type

Interventional

Funder types

Other

Identifiers

NCT02362763
VESTIB-HMO-CTIL

Details and patient eligibility

About

Randomized controlled trial designed to determine whether acupuncture is an effective treatment for vestibulitis.

Full description

Patients were randomized to five acupuncture sessions designed to treat pain in the vulvar area (study group), or five acupuncture sessions designed for tranquility (controls). Participants and evaluating gynecologists were blinded to randomization. Participants were examined clinically before treatment and one month after completion of assigned treatment; at both visits they completed the Female Sexual Function Index (FSFI) questionnaire.

FSFI scores for pain during intercourse and total score were used to evaluate change. The examining gynecologist evaluated the degree of sensitivity to touch and the degree of local erythema. Response to treatment was evaluated for each group before and after treatment, and for study group compared to the control group.

Enrollment

42 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Confirmed diagnosis of vestibulodynia

Exclusion criteria

  • Pregnancy
  • Patient who received other treatment for vestibulodynia in the month preceding.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

42 participants in 2 patient groups

Study group
Experimental group
Description:
Subjects received five acupuncture sessions designed to treat pain in the vulvar area
Treatment:
Procedure: Acupuncture
Controls
Active Comparator group
Description:
Controls received five acupuncture sessions designed for sedation
Treatment:
Procedure: Acupuncture

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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