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Doppler Ultrasound-Guided Angiopuncture for Dysmenorrhea Pain: A Clinical Trial

C

City University of Hong Kong

Status

Enrolling

Conditions

Dopplar Ultrasound
Angiopuncture
Dysmenorrhea

Treatments

Other: conduct angiopuncture on perforator points

Study type

Interventional

Funder types

Other

Identifiers

NCT07176910
111
9239056 (Other Grant/Funding Number)

Details and patient eligibility

About

the study is to evaluated dopplar guided angiopuncture efficacy and safety in patients with dysmenorrhea

Full description

to conduct angiopuncture, with dopplar located perforator points and also evaluate the spectrum before and after angiopuncture therapy.

Enrollment

30 estimated patients

Sex

Female

Ages

18 to 25 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

angiopuncture treated group
Experimental group
Description:
conduct angiopuncture therapy
Treatment:
Other: conduct angiopuncture on perforator points

Trial contacts and locations

1

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Central trial contact

Rong HAN, PhD student; Yuenkei LEE, Mphil

Data sourced from clinicaltrials.gov

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