Evaluation of Anti-mullerian Hormone(AMH) Levels as a Predictive Factor of Response to Weight Loss Treatment in Obese Infertile Women With Poly Cystic Ovary(PCOS)

Sponsor
Royan Institute (Other)
Overall Status
Completed
CT.gov ID
NCT01792362
Collaborator
(none)
60
1
1
18
3.3

Study Details

Study Description

Brief Summary

This study is a prospective before & after clinical trial to compare the basal and 3 months after diet anti-mullerian hormone levels between responders and non-responders to weight loss diet in obese infertile women with PCOS population

Condition or Disease Intervention/Treatment Phase
  • Other: Weight loss diet
Phase 3

Detailed Description

The study population comprised of all obese infertile PCOS patients aged 20-40 years which underwent 3 months weight loss diet in royan institute, Tehran Iran.

The study is conducted over 12 wk energy restriction. All subjects have the same dietary protocol. At baseline, week 12 the levels of AMH,Follicular Stimulating Hormone (FSH), Lutienizing Hormone(LH),Prolactin (PRL), androgens, sex hormone-binding globulin (SHBG), glucose, and insulin were measured and Free Androgen Index (FAI) and Insulin Resistance (IR) indices is calculated. The laboratory tests are determined by radioimmunoassay in the Laboratory of Endocrinology of Royan institute. AMH is measured in duplicate using an ultrasensitive ELISA kit (AMH-ELIZA Kit; Beckman Coulter, Marseilles, France) according to manufacturer instructions. All measurements are performed using a single kit and at the same time in the Laboratory of clinical Immunology of Royan institute.

Data collection will be performed by using questionnaire to be filled as per the available records and laboratory results. Data analysis will be done through descriptive and perceptive statistical methods.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparing the Basal Anti-mullerian Hormone Levels Between Responders and Non-responders to Weight Loss Diet in Obese Infertile Women With PCOS Population
Study Start Date :
Oct 1, 2012
Actual Primary Completion Date :
Nov 1, 2013
Actual Study Completion Date :
Apr 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: AMH

obese PCOS patients who underwent weight loss diet

Other: Weight loss diet
Control the patients diet to make them loosing weight

Outcome Measures

Primary Outcome Measures

  1. Blood level of AMH [3 months]

    Evaluation of Blood level of AMH 12 weeks after weight loss.

  2. Basal level of AMH [1 week]

    Evaluation the Basal level of AMH before starting weight loss diet

Secondary Outcome Measures

  1. Sensitivity of basal AMH level [6 months]

    Evaluation the Sensitivity of basal AMH level for predict the response to weight loss diet

  2. specificity of basal AMH level [6 months]

    Evaluation the specificity of basal AMH level for predict the response to weight loss diet

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 1- diagnosis of PCOS, according to the Rotterdam Consensus Workshop Group, by 2 of the following 3 criteria: menstrual irregularity (cycle length<26 d or >31 d or variation between consecutive cycles of >3 d); clinical (hirsutism assessed by a Ferriman-Gallwey score > 8) or biochemical [free androgen index (FAI) > 5.4 or testosterone_1.4 nmol/L] hyperandrogenism; or positive ultrasound presentation of polycystic ovaries by transvaginal scan.

2- Age between 18 -40

Exclusion Criteria:
    1. Body mass index (BMI; in kg/m2) < 30, 2. Type 2 diabetes mellitus and related endocrinopathic disorders [identified by assessment of thyroid-stimulating hormone (TSH), prolactin, and 17_hydroxyprogesterone].
  1. Regular exercise activities during the study. 4. Cases of alcoholism and smoking. 5. The use of endocrine hormonal treatment or insulin-sensitizing agents is not permitted during either phase of the study, and the use of oral contraceptives is not permitted during of the study. Subjects are required to cease taking oral contraceptives 4 wk and hormonal treatment or insulin-sensitizing agents 2 wk before commencement of the short-term study phase.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Royan Institute Tehran Iran, Islamic Republic of

Sponsors and Collaborators

  • Royan Institute

Investigators

  • Study Chair: Hamid Gourabi, PhD, Head of Royan Institute
  • Study Director: Ashraf Moini, MD, Department of Endocrinology and Female Infertility, Reproductive Biomedicine Center, Royan institute for Reproductive Biomedicine, ACECR, Tehran, Iran

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Royan Institute
ClinicalTrials.gov Identifier:
NCT01792362
Other Study ID Numbers:
  • Royan-Emb-015
First Posted:
Feb 15, 2013
Last Update Posted:
May 6, 2015
Last Verified:
Nov 1, 2012

Study Results

No Results Posted as of May 6, 2015