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Electroacupuncture added to metformin treatment in patients with polycystic ovary syndrome and overweight

Combination of electroacupuncture and pharmacological treatment in improving menstrual cycle and ovarian morphology in PCOS patients: double-blind randomized clinical trial

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN45111863
Enrollment
44
Registered
2020-08-18
Start date
2018-04-02
Completion date
Unknown
Last updated
2021-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polycystic ovarian syndrome Nutritional, Metabolic, Endocrine Polycystic ovarian syndrome

Interventions

Treatment group (EA Group): The patient receives adjuvant electroacupuncture. Sites used are the Zhongji (CV3), Guanyuan (CV4), Qihai (CV6), Tianshu (ST25), Shuidao (ST28), Zusanli (ST36), Chengsan (B

Sponsors

University of Indonesia and Cipto Mangunkusumo Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. 18 - 40 years old 2. BMI > 23kg/m² 3. Volunteering to join this research and giving informed consent

Exclusion criteria

Exclusion criteria: 1. Suffering from malignancy 2. Suffering from hypertension (blood pressure >140/90 mmHg, JNC 7 criteria) 3. Suffering from diabetes mellitus (fasting blood sugar >126 mg/dL, PERKENI 2015 criteria) 4. Currently in lactation 5. Suffering from endocrine disorders associated with steroid sex hormones such as congenital adrenal hyperplasia, Cushing’s syndrome, and androgen-secreting tumor diagnosed by a gynecologist 6. Currently undergoing pharmacological therapy related to dominant follicles stimulation such as clomiphene citrate, letrozole, FSH within 3 months 7. Subjects undergoing acupuncture therapy in the 12 weeks prior to recruitment 8. Subjects with absolute contraindications to electroacupuncture therapy such as: the first trimester of pregnancy, patients in a state of shock or coma, body temperature >38 degrees C, septicemia, tuberculosis of the skin or other local skin infection, heart rhythm disorders and patients with pacemakers, hypertension 9. Subjects with relative contraindications to electroacupuncture therapy such as: a history of epilepsy, pain and acute edema, and in patients with metal implants

Design outcomes

Primary

MeasureTime frame
1. Menstrual cycle length is measured in days using interview at baseline (before 1st session) and the end of acupuncture sessions (after 12th session) 2. Ovarian volume is measured in ml using transvaginal ultrasonography at baseline (before 1st session) and the end of acupuncture sessions (after 12th session) 3. Number of antral follicles is measured using transvaginal ultrasonography at baseline (before 1st session) and the end of acupuncture sessions (after 12th session)

Secondary

MeasureTime frame
Menstruation occurrence is measured using interview at baseline (before 1st session) and the end of acupuncture sessions (after 12th session)

Countries

Indonesia

Contacts

Public ContactWenny Kurniawan
wenikurniawan@yahoo.com+62 8559968686

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026