Furocyst - Poly Cystic Ovary Syndrome Study

NCT ID: NCT02703064

Last Updated: 2017-09-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

107 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-03-26

Study Completion Date

2017-07-31

Brief Summary

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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.

Detailed Description

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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.
3. 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 .
4. 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.

Conditions

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PCOS

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

open level
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Furocyst

Furocyst 500mg capsule, BD

Group Type EXPERIMENTAL

Furocyst

Intervention Type DIETARY_SUPPLEMENT

Furocyst caps BD

Interventions

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Furocyst

Furocyst caps BD

Intervention Type DIETARY_SUPPLEMENT

Other Intervention Names

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Standardized fenugreek extract

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Chemical Resources

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Dr. Pushpalata Sankhwar, M.S.

Role: PRINCIPAL_INVESTIGATOR

Dept of Obs & Gynae,King George's Medical University, Lucknow, UP, India

Locations

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Dept of Obs & Gynae, King George's Medical University, Lucknow, UP, India

Lucknow, Uttar Pradesh, India

Site Status

Countries

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India

References

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Polson DW, Adams J, Wadsworth J, Franks S. Polycystic ovaries--a common finding in normal women. Lancet. 1988 Apr 16;1(8590):870-2. doi: 10.1016/s0140-6736(88)91612-1.

Reference Type BACKGROUND
PMID: 2895373 (View on PubMed)

Other Identifiers

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Protocol No. CR-PCOS/1-15

Identifier Type: -

Identifier Source: org_study_id