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OpenTrials
Completed

NCT Number: NCT00873301

The Effectiveness of Vestibulectomy

Women with vulvodynia will fill out a questionnaire and undergo a gynecological examination before and 6 months after vestibulectomy. The investigators hypothesize that pain will decrease.

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Key information

Age range

18 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Western Galilee Hospital- Nahariya

Nahariya, 22100, Israel

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • vulvodynia, scheduled for vestibulectomy

Treatment and study plan

vestibulectomy

Procedure

Evaluation of the outcome of vestibulectomy which is the treatment of vulvar vestibulitis

Primary outcomes

  1. pain

    Time frame: 6 months following surgery

Secondary outcomes

  1. sexual function

    Time frame: 6 months afater surgery

Sponsors and collaborators

Lead sponsor

Western Galilee Hospital-Nahariya

Other Gov

Registry information

Important dates

Study start
2009
Primary completion
2012
Study completion
2012
First posted
Apr 1, 2009
Registry last updated
Apr 2, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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