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临床试验/CTRI/2026/02/104551
CTRI/2026/02/104551尚未招募2/3 期

Efficacy and safety of myoinositol vs combined hormonal pills along with metformin for dermatological symptoms of obese PCOS a randomized controlled trial.

Kalinga Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年3月20日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
入组人数
80
试验地点
1

研究概览

简要总结

Polycystic ovary syndrome PCOS is a common endocrine disorder affecting women of reproductive age and frequently presents with dermatological symptoms such as acne hirsutism androgenic alopecia and acanthosis nigricans. These cutaneous concerns have a major impact on appearance confidence and overall quality of life. Standard treatment for the skin manifestations of PCOS often includes combined hormonal pills to reduce androgen levels along with metformin to improve insulin resistance. Myoinositol is an emerging therapeutic option that also improves insulin sensitivity and may offer benefits in reducing androgenic symptoms with fewer side effects than hormonal therapy. However limited research has compared the effects of metformin combined with myoinositol against the established regimen of metformin combined with hormonal pills in obese PCOS patients specifically addressing skin outcomes.

This randomized controlled trial will compare the efficacy and safety of metformin plus myoinositol with metformin plus combined hormonal pills in obese women with PCOS who have moderate to severe dermatological manifestations. The study will be conducted in the Department of Dermatology at Kalinga Institute of Medical Sciences Bhubaneswar. Eighty participants will be enrolled and randomly allocated into two equal groups. One group will receive metformin 500 mg twice daily along with myoinositol 600 mg twice daily for three months. The other group will receive metformin 500 mg twice daily with a combined hormonal pill containing ethinyl estradiol and drospirenone for three treatment cycles.

Clinical severity of acne hirsutism alopecia and acanthosis nigricans will be evaluated using validated scoring tools at baseline and at three month follow up. Quality of life and patient satisfaction will also be assessed. Safety monitoring will include documentation of adverse effects and treatment tolerability in both groups. Data will be analyzed using standard statistical methods to compare changes within and between groups.

This study is expected to determine whether the combination of metformin and myoinositol provides superior improvement in dermatological symptoms and a better safety profile compared to the combination of metformin and hormonal pills. If successful this approach may offer an effective treatment alternative for obese PCOS patients who cannot tolerate hormonal therapy or prefer nonhormonal options.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
15.00 Year(s) 至 49.00 Year(s)(—)
性别
Female

入选标准

  • All Consenting Obese PCOS Female BMI more than equal to 25, Asia pacific guidelines, PCOS patients according to Rotterdam criteria with at least any one Cutaneous symptoms of moderate to severe variety like Acne with GAGS Score more than 18, Hirsutism with Modified Ferriman Gallwey Score more than 15, Female Pattern Hair Loss with Sinclair grade more than equal to 2 , Acanthosis Nigricans with Burke quantitative grade more than equal to 2).

排除标准

  • Pregnant or Lactating Woman, Diagnosed case of any other Endocrine Disorder Congenital Adrenal Hyperplasia, Hyperprolactinemia, Hypothyroidism or Systemic disorder, Diabetes with Vascular Complications, Recent hormonal therapy, Hepatic/renal dysfunction, Smokers, Patients on drugs that may interfere with CHP metabolism (e.g., Rifampicin, griseofulvin).

研究者

申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Ashneet Kaur Anand

Kalinga Institute of Medical Sciences

研究点 (1)

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