conduct angiopuncture on perforator points: conducted angiopuncutre on patients of intervention group, and compare those patients pain scores before and after angiopuncture therapy.
Study summary
the study is to evaluated dopplar guided angiopuncture efficacy and safety in patients with dysmenorrhea
Eligibility
Sex
FEMALE
Min age
18 Years
Max age
25 Years
Healthy volunteers
No
Inclusion Criteria:
Primary dysmenorrhea diagnosis (≥6 months of menstrual pain scoring ≥2 on numerical rating scale) Regular menstrual cycles (28-32 days), menstrual period lasts 4 to 7 days No pelvic pathology on transvaginal ultrasound.
Exclusion Criteria:
coagulopathy (INR \>1.5) recent analgesic use (48-hour washout) secondary dysmenorrhea confirmed by laparoscopy.
Primary outcome measure(s)
visual analog scale — pre-treatment, immediate post-treatment, check up 1, check up 2, check up 3 (3 check ups lasts for 3 months post therapy, with each for 1 month) to measure pain score before and after angiopuncture
Trial sites (1)
Facility
City
Region
Status
The Third Affiliated Hospital of Changchun University of Chinese Medicine
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
We use cookies to analyse site traffic and improve your experience. With your consent, we may also use cookies for advertising. You can change your choice at any time on our Cookie Policy page. See also our Privacy Policy.