Clinical Trial

Acupuncture in a Multidisciplinary Approach for Vulvodynia and Chronic Pelvic Pain

Study acronym: AMALIA
Recruiting
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Record status
This record was last updated December 12, 2024 (before its estimated January 2026 completion). Its status may not reflect the trial's current state.
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)
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2022-04-04; most recent amendment 2024-12-09.
Status change: Not Yet Recruiting → Recruiting 2022-06-24
Trial Details
NCT Number NCT05324280
Lead Sponsor Medical University of Graz
Conditions Vulvodynia, Chronic Pelvic Pain
Enrollment 68 participants
Start Date 2022-06-23
Primary Completion 2026-01 (estimated)
Study Completion 2026-07 (estimated)
Updated on ClinicalTrials.gov 2024-12-12