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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03546595
Other study ID # AA for IR-PCOS
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date July 1, 2018
Est. completion date December 31, 2020

Study information

Verified date December 2019
Source Heilongjiang University of Chinese Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The present trial is a pilot study to investigate the effect of auricular acupressure on insulin resistance in women with PCOS.A total of 100 subjects will be enrolled into this study and will be randomized into two groups.

Auricular acupressure or sham auricular acupressure will be treated for three months. The primary outcome is the whole body insulin action assessed with HOMA-IR.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 60
Est. completion date December 31, 2020
Est. primary completion date December 31, 2019
Accepts healthy volunteers No
Gender Female
Age group 15 Years to 40 Years
Eligibility Inclusion Criteria:

- Women aged between 15 and 40 years.

- Diagnosis of PCOS according to the modified Rotterdam criteria.

- 2 years after menarche.

- Body mass index (BMI) equal to or greater than 23 kg/m2.

- IR is defined by the homeostaticmodel assessment (HOMA-IR: (fasting insulin (µU/mL)×fasting glucose (mmol/L))/22.5). A value =2.14 will be considered to be indicative of IR.

- With no desire of children within 3 months.

Exclusion Criteria:

- Administration of other medications known to affect reproductive function or metabolism within the past three months, including oral contraceptives, Gonadotropin-releasing hormone (GnRH) agonists and antagonists, anti androgens, gonadotropins, anti-obesity drugs, Chinese herbal medicines, anti diabetic drugs such as metformin and thiazolidinediones, somatostatin, diazoxide, and calcium channel blockers.

- Patients with other endocrine disorders including 21-hydroxylase deficiency, hyperprolactinemia, uncorrected thyroid disease, suspected Cushing's syndrome.

- Patients with known severe organ dysfunction or mental illness.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Auricular acupoints acupressure
The magnetic beads were taped to the auricular acupressure points, by the same acupuncture specialist on one ear approximately after skin sterilization, and the subjects were asked to massage the points for 5 minutes, 30 minutes before three meals and sleep.The magnetic beads were left in situ, but replaced with new ones once every week in the other ear.
Sham auricular acupoints acupressure
The magnetic beads were taped to the auricular acupressure points, by the same acupuncture specialist on one ear approximately after skin sterilization, and the subjects were not asked to massage the points.The magnetic beads were left in situ, but replaced with new ones once every week in the other ear.

Locations

Country Name City State
China First Affiliated Hospital, Heilongjiang University of Chinese Medicine Harbin Heilongjiang

Sponsors (1)

Lead Sponsor Collaborator
Heilongjiang University of Chinese Medicine

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Homeostasis model assessment-insulin resistance (HOMA-IR) HOMA-IR was calculated as [Plasma glucose (GLU,mmol/L)* serum insulin (mIU/L)] / 22.5. 3 month
Secondary Testosterone(T) 3 month
Secondary Androstadienedione (AND) 3 month
Secondary Sex hormone-binding globulin (SHBG) 3 month
Secondary Dehydroepiandrosterone sulfate (DHEAS) 3 month
Secondary Follicle stimulating hormone (FSH) 3 month
Secondary Luteinizing hormone (LH) 3 month
Secondary Estradiol (E2) 3 month
Secondary Weight 3 month
Secondary Waist/hip circumference 3 month
Secondary BMI 3 month
Secondary FG score 3 month
Secondary Acne 3 month
Secondary Short-Form Health Survey (SF-36) 3 month
Secondary The Chinese Quality of Life questionnaire (ChQoL) 3 month
Secondary Health-related quality of life questionnaire for polycystic ovary syndrome (PCOSQ) 3 month
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