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NCT05972928CompletedPhase 2/3

Effect of Sitagliptin on Polycystic Ovarian Syndrome Patients

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

Source: ClinicalTrials.gov · Last updated 1 Sept 2026

Brief summary (registry, in English)

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

Status (registry)
Completed
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
80 (actual)
First submitted
25 Jul 2023
Start date
7 Aug 2024
Primary completion date
30 Apr 2025
Lead sponsor
Beni-Suef University
NCT number
NCT05972928

What you commit to

  • Study type: Interventional · Phase 2/3
  • Participants enrolled: 80
  • From 7 Aug 2024 to the primary completion date, 30 Apr 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Diabetic on Metformin or any another antidiabetic drugs affecting insulin resistance
  • documented use of oral hormonal contraceptives and hormone-releasing implants in the past 6 months prior to study entry 7.Lipid lowering Consumption

Other illness

  • Brittle control of a thyroid disorder
  • chronic kidney disease

Other

  • congenital adrenal hyperplasia
  • liver dysfunction

Who the study is looking for

  • polycystic ovary syndrome usually diagnosed based on the Rotterdam criteria if 2 of 3 criteria are present:
  • oligo- and/or anovulation
  • hyperandrogenism (HA) (clinical and/or biochemical)
  • polycystic ovary morphology (PCOM) on ultrasonography (either 12 or more follicles measuring 2-9 mm in diameter and/or an increased ovarian volume \>10 cm3).

Age in the registry: 20 years to 40 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Beni-Suef University Hospital
Coordinator of this site? Confirm its status
Banī SuwayfEgyptUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.