Furocyst - Poly Cystic Ovary Syndrome Study

Sponsor
Chemical Resources (Industry)
Overall Status
Completed
CT.gov ID
NCT02703064
Collaborator
(none)
107
1
1
27.2
3.9

Study Details

Study Description

Brief Summary

Poly cystic ovary syndrome (PCOS) is the most common endocrine disorder in women of reproductive age, affecting approximately 5%-10% of all females worldwide . PCOS is a hormonal disorder that involves multiple organ systems within the body. Its cardinal features are Hyperandrogenism and polycystic ovary (PCO) morphology. Women with PCOS may complains about irregular menstrual periods or heavy menstrual bleeding, infertility, excessive growth of coarse facial and body hair, obesity, oiliness of the skin, seborrhea, and cystic acne.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Furocyst
N/A

Detailed Description

The symptoms of PCOS are anovulation, resulting in irregular menstruation (amenorrhea and oligomenorrhea) ovulation-related infertility, and polycystic ovaries, often associated with obesity, Type 2 diabetes, and high cholesterol levels. The level of serum insulin and insulin resistance are higher in women with PCOS (Hyperinsulinemia).Insulin resistance, defined as the decreased insulin mediated glucose utilization it is more common in women with PCOS up to 50 % in both obese and non obese women . It has also been recognized that some women with this syndrome will have PCO without clinical evidence of androgen excess, but will display evidence of ovarian dysfunction .

It is believed to be that, the Hyperinsulinemia of PCOS stimulates the androgens production and increase the activity by decreasing the sex hormone binding globulin (SHBG) thus increasing the free active testosterone level and by the activating the cytochrome P 450 C 17 alpha enzymatic system that controls androgens production.

The diagnosis of PCOS is based on Hyperandrogenism and chronic anovulation in the absence of specific pituitary or adrenal disease , and have disrupted ovulatory function with chronic oligomenorrhea (cycle length > 35 day) or amenorrhea (cycle length > 12 week) and typical appearance of polycystic ovaries by ultrasound according to the criteria of the Rotterdam consensus meeting 2003 for diagnosis of PCOS. The different diagnostic tests needed to adequately assess for the possibility of PCOS e.g. Pregnancy test, TSH level (for Hyperthyroidism), Prolactin test (for Hyperprolactinemia), Total testosterone (for ovarian tumor) and some tests forevaluating the insulin resistance syndrome in women: Waist circumference (>88 cm), Triglycerides (>150 mg/dL), HDL Cholesterol (<50 mg/dL), Blood pressure (>130/85) and Fasting glucose (>110 mg/dL). Fasting glucose- to- insulin ratio and 2 hour oral glucose tolerance test (2h- OGTT 140 - 199 mg/dL) may be better predictor of insulin resistance .

The management of the PCOS is symptoms specific e.g.

  1. Oral contraceptives, periodic progesterone withdrawal for the control of irregular menstruation.

  2. Oral contraceptives, Metformin and anti-androgens (Spironolactone) for the

Hirsutism.

  1. Clomiphene citrate, Metformin and thiazolidinediones for infertility. A recent study shown that, the combination of Metformin plus Clomiphene citrate should be considered as the First line treatment for infertile women with PCOS .

  2. Metformin and lifestyle modification for the insulin resistance and diabetes mellitus.

All these management options are only for "acute" not for "chronic". The long-term management approach for the PCOS is needed which will be based on management of most affecting factor insulin resistance.

Study Design

Study Type:
Interventional
Actual Enrollment :
107 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
open levelopen level
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
To Study the Efficacy and Safety of Furocyst in Poly Cystic Ovary Syndrome Patients (PCOS)
Actual Study Start Date :
Mar 26, 2015
Actual Primary Completion Date :
Jul 1, 2017
Actual Study Completion Date :
Jul 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Furocyst

Furocyst 500mg capsule, BD

Dietary Supplement: Furocyst
Furocyst caps BD
Other Names:
  • Standardized fenugreek extract
  • Outcome Measures

    Primary Outcome Measures

    1. Reduction in Overian volume & Number of overian Cysts [12 weeks]

    Secondary Outcome Measures

    1. Restoration of normal menstrual cycle [12 weeks]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Premenopausal women between 18-45 years of age and BMI less than 42

    • Diagnosed with PCOS by Rottadom Criteria

    • Adequate hepatic, renal, Cardiac and hematological functions.

    • Patients willing to Participate and give informed consent in writing as well as in audio-visual form for the study.

    • Stable weight for last two months (Change of weight<3kg)

    Exclusion Criteria:
    • Male

    • Post menopausal women

    • Women with hysterectomy

    • Hyperprolactinemia

    • Patients with congenital adrenal hyperplasia

    • Patients suffering from Cushing's syndrome

    • Acute or chronic Medical illness including Hepatic, Cardiac or renal insufficiency, COPD,Gastrointestinal Disorders

    • Uncontrolled Hypertensive or known Diabetics on drugs

    • Use of oral contraceptives or HRT for last three months

    • Smoking or drug addicts or with psychiatric illness

    • Patients diagnosed with androgen secreting tumors.

    • Patients with thyroid dysfunction (T3, T4 level is higher than that in normal women of reproductive age)

    • Patients with Hypo-gonadotropic and Hypo-gonadism (central origin of ovarian dysfunction)

    • Pregnant or lactating mothers

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Dept of Obs & Gynae, King George's Medical University, Lucknow, UP, India Lucknow Uttar Pradesh India 226003

    Sponsors and Collaborators

    • Chemical Resources

    Investigators

    • Principal Investigator: Dr. Pushpalata Sankhwar, M.S., Dept of Obs & Gynae,King George's Medical University, Lucknow, UP, India

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Chemical Resources
    ClinicalTrials.gov Identifier:
    NCT02703064
    Other Study ID Numbers:
    • Protocol No. CR-PCOS/1-15
    First Posted:
    Mar 9, 2016
    Last Update Posted:
    Sep 15, 2017
    Last Verified:
    Aug 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Chemical Resources
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 15, 2017