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临床试验/NCT02744131
NCT02744131Unknown不适用

OCP vs Metformin for Improvement in Clinical Symptoms and Metabolic Markers in Indian PCOS Women

Kar Clinic & Hospital Pvt. Ltd.1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2016年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
100
试验地点
1
主要终点
Improvement in acne score

研究概览

简要总结

Objective: To assess effectiveness of ISD (Insulin sensitizing drugs) Vs OCP (Combined E&P cyproterone acetate) in improving clinical, hormonal and metabolic features of PCOS( polycystic ovary syndrome)women from India.

Intervention:

Randomized to receive Metformin 1500 mg / day OR OCP (EE+CA) Life style advice to women with BMI ( body mass index) more than 28 , in both groups (PS: progesterone can be added for getting withdrawal bleeding for amenorrhoea of more than two months, or for prolonged menstrual bleeding. ) Study period: 6 months Clinical evaluation points and tests at enrollment and again after 6 month. Clinical: BMI, Waist circumference, Hip circumference, Acne score, FG (modified Ferriman Gallwey score ) (after no epilation for last 6 weeks), Menstrual History Biochemical: Thyroid function tests, Prolactin,Total Testosterone, Lipid Profile, FAsting blood sugar & 75 gm 2 hr Glucose tolerance test (GTT), Sr Insulin, 25- hydroxy vitamin D (optional), (Only Radioimmunoassay / Chemiluminescence assays)

Acronyms: OCP(oral contraceptive pills); PCOS (polycystic ovary syndrome); FBS(fasting blood sugar); GTT(glucose tolerance test)

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
16 Years 至 40 Years(Child, Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •PCOS Women diagnosed by Rotterdam criteria
  • •Age > 16 or menarche of at least 2 yr upto age
  • •Diagnosed by Rotterdam Anovulation F.G. Score ≥ 8 or Total testosterone ≥ 40 ngms/dl ovarian volume ≥ 10 cc BMI>23
  • •Women not attempting pregnancy at present.

排除标准

  • •PCOS Women with BMI ≤ 23
  • •Undergoing any treatment for acne hirsutism. Including Homeopathic, Ayurvedic
  • •Known diabetic or hypertension .

研究组 & 干预措施

Metformin

Active Comparator

Arm 2: Metformin . Oral insulin sensitising drug in the dose of 1500gms daily.

干预措施: Metformin 1500mgs per day (Drug)

OCP

Active Comparator

Arm 1: oral contraceptive pill, combination pill of ethyl estradiol 20 micro gram with Cyproterone acetate.

干预措施: Oral contraceptive pill combination of ethyl estradiol and Cyproterone acetate (Drug)

结局指标

主要结局

Improvement in acne score

时间窗: Six months

Acne scores before and after treatment will be compared between the two arms. Visual assessment of acne using "mild/moderate/severe " grades will be assessed before and after study by a physician.

Reduction in serum fasting insulin

时间窗: 6 months

Reduction in insulin levels following treatment will be compared between the two arms

Improvement in glucose tolerance

时间窗: 6months

75grams 2 hour glucose challenge test results will be compared pre and post treatment between the two groups

Weight loss following treatment

时间窗: 6months

Weight loss will be compared between the two arms following 6 months of treatment

Improvements in Menstrual cycle in women with polycystic ovary syndrome.

时间窗: Six months

To compare improvement in Menstrual cycle. Women will be required to maintain a menstrual calendar for the duration of the study and asked to fill a questionnaire before and after study duration.The questionnaire will cover menstrual cycle dates, duration and amount. Interpreting the answered will help in assessing improvement in menstrual pattern.

Reduction in total testosterones

时间窗: 6months

Reduction in total testosterones, signifying biochemical hyperandrogenemia, will be compared between the two groups following 6 months treatment.

Improvements in lipid profile

时间窗: 6months

Any improvement in triglycerides and HDLc (high density lipoprotein c) will be compared between the two groups after 6 months of treatment

Improvement in hirsutism

时间窗: six months

FG scores before and after treatment will be compared between the two arms. Modified Ferriman and Gallwey visual score will be used by a nurse to assess before and after the study period.

次要结局

未报告次要终点

研究者

发起方
Kar Clinic & Hospital Pvt. Ltd.
申办方类型
Other
责任方
Sponsor

研究点 (1)

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