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nderstanding the prevalence ,risk factors, and drug responses to polycystic ovary syndrome among Indian Women.

Phase 4
Completed
Conditions
Health Condition 1: E898- Other postprocedural endocrine andmetabolic complications and disorders
Registration Number
CTRI/2018/11/016252
Lead Sponsor
SKIMS
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1) Women aged 18-40 years.

2) Women permanent residents of that area ( >1 year).

3) Willingness to participate in the study and sign informed consent.

4) Women who are known to have PCOS not on treatment.

Exclusion Criteria

1) Pregnant or lactating women and those with cognitive and/or physical limitations that prevented them from answering the questionnaire will be excluded from the study.

2) History of drug intake such as steroids, androgen, oral contraceptives, anti-epileptics or drugs known to interfere in glucose and lipid metabolism.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
a)Estimation of national prevalence, phenotypic variations and risk factors of PCOS in community. <br/ ><br>b)Quantitation of comorbidities among known cases of PCOS <br/ ><br>c)Comparison of the variation in efficacy of standard therapeutics modalities for metabolic dysfunction in PCOS women <br/ ><br>Timepoint: Baseline and follow up at the interval of 3 month and 6 month
Secondary Outcome Measures
NameTimeMethod
a)Identification of prenatal/pre-pubertal factors including low birth weight, sexual precocity, pre-pubertal obesity, familial aggregation, maternal PCOS, GDM, antiepileptic drug, etc. contributing in the causation of PCOS. <br/ ><br>b)Assessment of knowledge and management practices among service providers in public health sector on PCOSTimepoint: Baseline,
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