Myo-inositol vs Metformin for Obesity Treatment in PCOS Patients
This study aims to compare the effectiveness of Myo-inositol and Metformin in reducing body mass index as a treatment for obesity in patients with Polycystic Ovary Syndrome (PCOS).
Myo-inositol
+ Metformin
Urogenital Diseases+10
+ Genital Diseases
+ Adnexal Diseases
Treatment Study
Summary
Study start date: November 29, 2024
Actual date on which the first participant was enrolled.This study focuses on comparing two treatments, myo-inositol and metformin, for managing obesity in patients with Polycystic Ovarian Syndrome (PCOS). The aim is to understand which treatment works better and is more tolerable for these patients. PCOS is a common health condition that can lead to obesity and other metabolic disorders. This research is important as it can help gynecologists make more informed decisions when choosing medications for their patients, potentially improving their quality of life and reducing psychological impacts associated with obesity, such as discrimination and low self-esteem. During the study, participants receive either myo-inositol or metformin as their treatment. The main goal is to measure the reduction in body mass index (BMI) from the start of the study. This helps determine the effectiveness of each treatment. The study also considers the side effects of each medication to understand which one is more tolerable for patients with PCOS.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.60 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 18 to 45 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location