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NCT00874484 Clinical Trial

Enoxaparin as Treatment for Vulvodynia

Vulvodynia Clinical Trial

Official title:
Enoxaparin as Treatment for Vulvar Vestibulitis Syndrome - Vulvodynia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00874484
Other study ID # JB 2409
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date March 2009
Est. completion date May 2011

Study information
Verified date May 2020
Source Western Galilee Hospital-Nahariya
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators hypothesize that injections of Low molecular weight heparin (LMWH) [enoxaparin] will reduce pain in women with vulvodynia.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date May 2011
Est. primary completion date April 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 19 Years to 50 Years
Eligibility Inclusion Criteria:

- women with vulvodynia

Exclusion Criteria:

- women without vulvodynia

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Clexane (enoxaparin)
One arm receives enoxoparin, second arm receives saline

Locations
Country Name City State
Israel Western Galilee Hospital- Nahariya Nahariya

Sponsors (1)
Lead Sponsor Collaborator
Western Galilee Hospital-Nahariya

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary vestibular pain one year
See also
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Terminated NCT04016467 - Effect of Spinal Manipulation on Vulvar Pain N/A
Completed NCT01935063 - Study to Compare the Efficacy of Cognitive-behavioral Couple Therapy and Lidocaine for Provoked Vestibulodynia N/A
Completed NCT02809612 - An Internet-based Information Platform for Vulvodynia Patients N/A