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Spots Global Cancer Trial Database for Effect of Sitagliptin on Polycystic Ovarian Syndrome Patients

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Trial Identification

Brief Title: Effect of Sitagliptin on Polycystic Ovarian Syndrome Patients

Official Title: Effect of Sitagliptin on Clinical, Metabolic and Hormonal Parameters in Polycystic Ovarian Syndrome Patients

Study ID: NCT05972928

Interventions

Sitagliptin 100mg

Study Description

Brief Summary: The Study aims to determine the proposed positive influence of Sitagliptin in manipulating hormonal , metabolic and inflammatory parameters in the treatment of Polycystic ovary syndrome and subsequent infertility

Detailed Description: Study Design : a Prospective Randomized Controlled Trial. A Total of 80 infertile Adult Females aged between 18 and 45 years currently diagnosed with Polycystic ovary syndrome , Meeting the Diagnosis of Rotterdam criteria be diagnosed if any two of the following are present: (1) clinical or biochemical hyperandrogenism, (2) evidence of oligo-anovulation, (3) polycystic appearing-ovarian morphology on ultrasound are to be included in the study. The study will include two groups; each group consists of 40 patients:- Group A : Control Group Group B : Test Group ( will Receive Sitagliptin at a dose of 100 mg every 24 hours

Eligibility

Minimum Age: 20 Years

Eligible Ages: ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Beni-suef university Hospital, Banī Suwayf, Beni Suef, Egypt

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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