Last updated: February 1, 2024
Sponsor: Medipol University
Overall Status: Active - Recruiting
Phase
N/A
Condition
Interstitial Cystitis
Bladder Disorders
Urinary Incontinence
Treatment
ACUPUNCTURE
Clinical Study ID
NCT06232200
34043404
Ages 30-65 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- who diagnosed IC/BPS
- between 30-65 years old
- female
Exclusion
Exclusion Criteria:
- Patients who do not meet the IC/BPS diagnostic criteria,
- who have previously received acupuncture treatment,
- who have localized skin infections involving the acupuncture areas,
- who have bleeding diathesis and who use anticoagulant drugs,
- who cannot comply with the treatment and follow-up schedule will not be included inthe study.
Study Design
Total Participants: 26
Treatment Group(s): 1
Primary Treatment: ACUPUNCTURE
Phase:
Study Start date:
January 01, 2024
Estimated Completion Date:
January 01, 2025
Connect with a study center
istanbul Çam Sakura city hospital
Istanbul,
TurkeyActive - Recruiting
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