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Clinical Trial Summary

Background: Vulvodynia and chronic pelvic pain (CPP) are common and challenging gynecologic pain syndromes. A multidisciplinary approach is recommended. Study aim: To study the effectiveness of acupuncture as part of a multimodal treatment for women with vulvodynia and CPP. Design: Randomised controlled clinical study Study Population: Recruitment from a University outpatient clinic Study groups: Participants will be randomised (1:1) - Acupuncture group - Waiting list control group Sample size: 68 patients Study outcome - Subjective Pain Perception (VAS) - Health-related quality of life (questionnaires)


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT05324280
Study type Interventional
Source Medical University of Graz
Contact
Status Recruiting
Phase N/A
Start date June 23, 2022
Completion date July 2025

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