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Completed

NCT Number: NCT03008551

Empagliflozin vs Metformin in PCOS

This a randomised open-label parallel study involving women with polycystic ovary syndrome (PCOS). The patients will be randomised either to metformin 1500mg or empagliflozin 25mg daily for three months. The aim of the study is to examine the effect of empagliflozin on hormonal, metabolic and cardiovascular risk markers and quality of life in women with PCOS.

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Michael White Centre for Diabetes and Endocrinology

Hull, East Yorkshire, HU3 2RW, United Kingdom

About this study

Polycystic ovary syndrome (PCOS) is a very common condition in women that may present with irregular periods, excessive hair growth on the face and body, acne and cysts in the ovaries. PCOS is also associated with increased risk of problems later in life like diabetes, high cholesterol levels and heart disease.

In this study, a medication named Empagliflozin will be tested. Empagliflozin belongs to a class of medicines known as SGLT-2 inhibitors. SGLT-2 stands for sodium glucose co-transporter 2. Empagliflozin, in simple terms, helps in reducing high blood glucose levels by increasing the amount of glucose passed in your urine. This medicine is usually used in patients with type 2 diabetes and has led to improved blood pressure and weight loss in addition to improving blood glucose levels.

We want to give Empagliflozin to women with PCOS to see its effect on hormones related to PCOS and the risk factors for diabetes and heart disease. We will be comparing its effects to metformin (another drug for diabetes) which has already been used in PCOS with very good results.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women, aged 18-45 years (inclusive), with confirmed diagnosis of PCOS based on Rotterdam criteria.
  • Presence of both irregular periods and biochemical hyperandrogenaemia
  • Body mass index ≥25
  • Negative pregnancy test during screening visit and agree to use barrier contraception during the study period.

Exclusion criteria

  • Non-classical 21-hydroxylase deficiency, hyperprolactinaemia, Cushing's disease and androgen-secreting tumours will be excluded by appropriate tests.
  • Confirmed diagnosis of diabetes or pre-diabetes.
  • Ongoing, inadequately controlled thyroid disorder (subjects on thyroid hormone replacement therapy must be on stable dose for at least 3 months before screening day)
  • History or presence of malignant neoplasms within the last 5 years (except basal and squamous cell skin cancer and in-situ carcinoma).
  • History or plan of any form of gastrointestinal tract surgery.
  • History of pancreatitis (Acute or Chronic).
  • Any disorder which in the opinion of the investigator might jeopardize subject's safety.
  • Subjects who are on any of the following medications within 3 months of recruitment:
  • Metformin or other insulin-sensitizing medications (e.g., pioglitazone )
  • Hormonal contraceptives (e.g., birth control pills, hormone-releasing implants, etc.)
  • Anti-androgens (e.g., spironolactone, flutamide, finasteride, etc.)
  • Clomiphene citrate or estrogen modulators such as letrozole
  • GnRH modulators such as leuprolide
  • Minoxidil
  • Female who is pregnant, breast feeding or intended to become pregnant or of child bearing potential not using adequate contraceptive methods.
  • eGFR<60
  • Hypersensitivity to lactose
  • Severe hepatic impairment (ALT >3 times ULN)
  • Women with history of recurrent urinary tract infections.
  • Haematocrit above the upper limit of normal range.
  • Have been involved in another medicinal trial (CTIMP) within the past four weeks.
  • Known hypersensitivity to the Investigational Medicinal Products or any of their excipients.

Treatment and study plan

Empagliflozin

Drug

Each participant will receive empagliflozin 25mg daily for 3 months.

Other names: Jardiance

metformin

Drug

Each participant will receive metformin 1500mg daily for 3 months.

Other names: Glucophage SR

Primary outcomes

  1. Endothelial function as measured by RHI (reactive hyperaemia index).

    Time frame: Three months treatment with either empagliflozin 25mg or metformin 1500mg daily

    Endothelial function as measured by RHI (reactive hyperaemia index) will be assessed after three months treatment with either empagliflozin 25mg or metformin S/R 1500mg daily

Secondary outcomes

  1. Inflammatory markers (hsCRP)

    Time frame: Three months treatment with either empagliflozin 25mg or metformin 1500mg daily

    Inflammatory markers (hsCRP) will be assessed after three months treatment with either empagliflozin 25mg or metformin S/R 1500mg daily

  2. Insulin resistance as measured by HOMA (fasting glucose & insulin)

    Time frame: Three months treatment with either empagliflozin 25mg or metformin 1500mg daily

    Insulin resistance as measured by HOMA (fasting glucose & insulin) will be assessed after three months treatment with either empagliflozin 25mg or metformin S/R 1500mg daily

  3. Body weight

    Time frame: Three months treatment with either empagliflozin 25mg or metformin 1500mg daily

    Body weight will be assessed after three months treatment with either empagliflozin 25mg or metformin S/R 1500mg daily

  4. Blood pressure

    Time frame: Three months treatment with either empagliflozin 25mg or metformin 1500mg daily

    Blood pressure will be assessed after three months treatment with either empagliflozin 25mg or metformin S/R 1500mg daily

  5. Lipid profile

    Time frame: Three months treatment with either empagliflozin 25mg or metformin 1500mg daily

    Lipid profile will be assessed after three months treatment with either empagliflozin 25mg or metformin S/R 1500mg daily

  6. Hormonal parameters including free androgen index

    Time frame: Three months treatment with either empagliflozin 25mg or metformin 1500mg daily

    Hormonal parameters including free androgen index will be assessed after three months treatment with either empagliflozin 25mg or metformin S/R 1500mg daily

  7. Endothelial function measured by microparticles

    Time frame: Three months treatment with either empagliflozin 25mg or metformin 1500mg daily

    Endothelial function measured by microparticles will be assessed after three months treatment with either empagliflozin 25mg or metformin S/R 1500mg daily

  8. Quality of life Questionnaire

    Time frame: Three months treatment with either empagliflozin 25mg or metformin S/R 1500mg daily

    Quality of life will be assessed after three months treatment with either empagliflozin 25mg or metformin S/R 1500mg daily

Sponsors and collaborators

Lead sponsor

Hull University Teaching Hospitals NHS Trust

Other Gov

Registry information

Official study title

The Effect of Empagliflozin Versus Metformin on Hormonal, Metabolic and Cardiovascular Risk Factors in Patients With Polycystic Ovary Syndrome (PCOS) - a Randomised Open-label Parallel Study.

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Jan 2, 2017
Registry last updated
Jul 15, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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