Efficacy and Safety of Metformin versus Myoinositol in improving Clinicometabolic profile in patients diagnosed with Polycystic Ovary syndrome: A Randomized Controlled trial
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 126
- 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 is frequently associated with insulin resistance, menstrual irregularities, hyperandrogenism, and metabolic abnormalities. Metformin is widely used as an insulin-sensitizing agent for the management of PCOS; however, its use may be limited due to gastrointestinal side effects and poor patient adherence. Myo-inositol, a naturally occurring insulin sensitizer involved in insulin signaling pathways, has emerged as a potential alternative therapy with fewer adverse effects.This study aims to compare the efficacy and safety of myo-inositol and metformin in improving the clinicometabolic profile among women diagnosed with PCOS. The study will be conducted as an open-label randomized controlled trial at AIIMS Patna and will include 126 women aged 18–40 years diagnosed with PCOS according to the Rotterdam criteria. Participants will be randomly allocated in a 1:1 ratio to receive either myo-inositol 1 g twice daily or metformin 500 mg twice daily for one week followed by thrice daily dosing for a total duration of 24 weeks.The primary outcome will be the change in insulin resistance measured by HOMA-IR score at 12 weeks. Secondary outcomes will include changes in HOMA-IR at 24 weeks, lipid profile, body mass index, menstrual cycle regularity, acne, hirsutism, and treatment tolerability. The findings of this study may help determine whether myo-inositol can serve as an effective and safer alternative to metformin for the management of PCOS.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 40.00 Year(s)(—)
- 性别
- Female
入选标准
- •Women aged 18-40 years.
- •Diagnosed with PCOS as per Rotterdam criteria 3.Willing to participate and provide written informed consent.
- •Patients not planning to get pregnant in 6 months.
排除标准
- •Women with diabetes mellitus, thyroid disorders, or hyperprolactinemia.
- •Use of hormonal therapy, insulin sensitizers, or ovulation-inducing drugs within the last 3 months
- •Patients seeking treatment for infertility
- •Known liver, renal, or cardiovascular disease.
- •Pregnant or lactating women.
- •Hypersensitivity or intolerance to study medications.
研究者
Dr Priya Kumari
AIIMS Patna
