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Furocyst - Poly Cystic Ovary Syndrome Study

To Study the Efficacy and Safety of Furocyst in Poly Cystic Ovary Syndrome Patients (PCOS)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02703064
Enrollment
107
Registered
2016-03-09
Start date
2015-03-26
Completion date
2017-07-31
Last updated
2017-09-15

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

Conditions

PCOS

Keywords

Furocyst, PCOS

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.

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. 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.

Interventions

DIETARY_SUPPLEMENTFurocyst

Furocyst caps BD

Sponsors

Chemical Resources
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

open level

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
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

Design outcomes

Primary

MeasureTime frame
Reduction in Overian volume & Number of overian Cysts12 weeks

Secondary

MeasureTime frame
Restoration of normal menstrual cycle12 weeks

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026