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临床试验/NCT07747909
NCT07747909招募中不适用

Effect of Orlistat on Metabolic and Hormonal Features in Women With Polycystic Ovary Syndrome (PCOS): a Randomized Controlled Clinical Trial

Khyber Medical University Peshawar1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2026年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
120
试验地点
1
主要终点
Polycystic Ovary Syndrome (PCOS) Features

研究概览

简要总结

This randomized controlled clinical trial aims to evaluate the effect of orlistat on the metabolic and hormonal features of women with polycystic ovary syndrome (PCOS). Eligible women diagnosed with PCOS according to the Rotterdam criteria will be randomly assigned to receive either orlistat plus standard lifestyle advice or placebo plus standard lifestyle advice for three months. The study will assess the effect of orlistat on hormonal parameters, glucose metabolism, lipid profile, liver function, anthropometric measures, non-alcoholic fatty liver disease, and quality of life to determine its effectiveness as an adjunctive treatment for women with PCOS.

详细描述

Polycystic ovary syndrome (PCOS) is one of the most common endocrine and metabolic disorders affecting women of reproductive age and is frequently associated with obesity, insulin resistance, dyslipidemia, and hormonal imbalance. Lifestyle modification remains the cornerstone of management; however, additional therapeutic options are needed to improve metabolic and reproductive outcomes. Orlistat, a gastrointestinal lipase inhibitor, promotes weight reduction by decreasing dietary fat absorption and has demonstrated potential benefits in improving insulin resistance and lipid metabolism.

This study is a single-center, randomized controlled clinical trial to be conducted at Ayub Teaching Hospital, Abbottabad. A total of 120 women aged 18-45 years with PCOS diagnosed according to the Rotterdam criteria will be enrolled and randomly allocated in a 1:1 ratio to either the intervention group or the control group. Participants in the intervention group will receive orlistat capsules twice daily in addition to standard lifestyle advice, while participants in the control group will receive placebo together with the same lifestyle recommendations, including a healthy diet and regular physical activity. The intervention period will last three months.

Participants will undergo baseline assessment, telephone follow-up visits at one and two months to monitor treatment adherence, and a final in-person assessment after three months. The primary outcome is improvement in at least one abnormality defined by the Rotterdam diagnostic criteria. Secondary outcomes include changes in sex hormone profile (LH, FSH, LH/FSH ratio, AMH, and free testosterone), fasting glucose and insulin parameters, HbA1c, lipid profile, liver function tests, lipid accumulation product, hepatic steatosis index, ultrasound grading of non-alcoholic fatty liver disease, anthropometric measures, and PCOS-related quality of life. The findings of this study will provide evidence regarding the effectiveness of orlistat as an adjunct to lifestyle modification for improving the metabolic and hormonal manifestations of PCOS in women.

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

盲法说明

Participants will be blinded to treatment allocation. Participants in the intervention and control groups will receive identical-appearing capsules (Orlistat or placebo). Care providers, investigators, and outcome assessors will not be blinded to group assignment.

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Females aged 18-45 years.
  • Diagnosis of polycystic ovary syndrome (PCOS) according to the Rotterdam Criteria (presence of any two of the following):
  • Oligomenorrhea or amenorrhea.
  • Clinical or biochemical hyperandrogenism.
  • Polycystic ovaries on ultrasonography.
  • Body mass index (BMI) between 18.5 and 35 kg/m² (Asian criteria).

排除标准

  • Current or recent use of oral contraceptives, ovulation induction medications, anti-obesity medications, cholesterol-lowering medications, or other therapies/supplements known to affect insulin physiology or androgen metabolism (e.g., inositols, curcumin, lipoic acid, cinnamon, gymnemic, or other botanical extracts).
  • Women undergoing in vitro fertilization (IVF) treatment.
  • Known congenital adrenal hyperplasia, thyroid disorders, hyperprolactinemia, or diabetes mellitus.
  • Presence of severe renal or liver disease.
  • Menopausal, pregnant, or breastfeeding women.
  • Anti-Müllerian Hormone (AMH) < 0.7 ng/mL.

研究组 & 干预措施

Orlistat + Standard Lifestyle Advice

Experimental

Participants will receive oral Orlistat capsules twice daily between lunch and dinner for 3 months in addition to standard lifestyle advice, including a healthy diet, regular physical activity, walking or cycling for at least 30 minutes daily, and other lifestyle modifications.

干预措施: Standard Lifestyle Advice (Behavioral)

Placebo + Standard Lifestyle Advice

Placebo Comparator

Participants will receive matching placebo capsules twice daily for 3 months together with the same standard lifestyle advice, including a healthy diet, regular physical activity, walking or cycling for at least 30 minutes daily, and other lifestyle modifications

干预措施: Placebo (Drug)

Placebo + Standard Lifestyle Advice

Placebo Comparator

Participants will receive matching placebo capsules twice daily for 3 months together with the same standard lifestyle advice, including a healthy diet, regular physical activity, walking or cycling for at least 30 minutes daily, and other lifestyle modifications

干预措施: Standard Lifestyle Advice (Behavioral)

Orlistat + Standard Lifestyle Advice

Experimental

Participants will receive oral Orlistat capsules twice daily between lunch and dinner for 3 months in addition to standard lifestyle advice, including a healthy diet, regular physical activity, walking or cycling for at least 30 minutes daily, and other lifestyle modifications.

干预措施: Orlistat (Drug)

结局指标

主要结局

Polycystic Ovary Syndrome (PCOS) Features

时间窗: Baseline and 3 months

Improvement in at least one baseline abnormality according to the Rotterdam Criteria, including ovulatory dysfunction, hyperandrogenism, or polycystic ovarian morphology on ultrasonography.

Luteinizing Hormone/Follicle Stimulating Hormone (LH/FSH) Ratio

时间窗: Baseline and 3 months

Change in serum LH/FSH ratio measured by laboratory assay. Higher values indicate greater hormonal imbalance.

Anti-Müllerian Hormone (AMH)

时间窗: Baseline and 3 months

Change in serum Anti-Müllerian Hormone concentration (ng/mL) measured by laboratory assay.

Follicle Stimulating Hormone (FSH)

时间窗: Baseline and 3 months

Change in serum FSH concentration (IU/L) measured by laboratory assay

Luteinizing Hormone (LH)

时间窗: Baseline and 3 months

Change in serum LH concentration (IU/L) measured by laboratory assay.

Free Testosterone

时间窗: Baseline and 3 months

Change in serum free testosterone concentration measured by laboratory assay.

Fasting Blood Glucose

时间窗: Baseline and 3 months

Change in fasting blood glucose concentration (mg/dL) measured by laboratory assay.

次要结局

未报告次要终点

研究者

发起方
Khyber Medical University Peshawar
申办方类型
Other
责任方
Sponsor

研究点 (1)

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