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Completed

NCT Number: NCT03086005

Study to Assess the Effect of Metformin Supplementation on IVF Outcome in Patients With Polycystic Ovarian Syndrome.

This study was performed to investigate the effects of metformin on controlled ovarian stimulation (COS), in vitro fertilization (IVF) outcomes, pregnancy outcomes, and comparison of serum and follicular fluid cytokines and hormones in patients with polycystic ovary syndrome (PCOS) undergoing IVF using gonadotropin-releasing hormone(GnRH) antagonist protocol.

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Key information

Age range

20 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Asan Medical Center

Seoul, Songpa-gu, 05505, South Korea

About this study

Polycystic ovary syndrome is the common cause of the female infertility that features insulin resistance and hyperinsulinemia participate in the reproductive as well as metabolic disturbances.

In many studies, metformin treatment reduces androgen levels and attenuates hyperinsulinemia in women with PCOS. This favorable effect on insulin and androgens levels, justifies the use of metformin in reproductive disturbances in PCOS women. Metformin treatment was shown to diminish ovarian androgen secretion, while lowering insulin levels in women with PCOS.

In women with PCOS, metformin treatment may increase ovulation, improve menstrual cyclicity, and reduce seum androgen levels. Metformin has direct effects on the ovary and also reduces the level of insulin that act upon the ovary. It has been indicated that metformin has direct, insulin-independent actions on theca cell steroidogenesis, because in human ovarian theca-like tumor cells, metformin suppressed androstenedione production. Metformin also exert a direct effect on granulosa cells and subsequent reduction of steroid production.

Metformin was shown to improve endothelium dependent vasodilation in insulin resistant patients and potentially protect against atherogenesis and cardiovascular disease.

Considering gonadotropin ovulation induction or IVF in women with PCOS, metformin coadministration improves the pregnancy outcome and reduces the risk of ovarian hyperstimulation syndrome. Metformin therapy throughout pregnancy can reduce the risk of early miscarriage or the incidence of gestational diabetes.

All patients were pretreated for 3 weeks with monophasic oral contraceptive (OC)(Yasmin; Bayer Schering Pharma, Berlin, Germany) before COS. Five days after OC discontinuation, COS for IVF/ICSI was commenced. GnRH antagonist protocol was used for COS in all subjects. Patients were randomly allocated into the metformin or control groups, using sealed envelopes.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • PCOS diagnostic criteria
  • 2003 American Society for Reproductive Medicine(ARSM)/European Society of Human Reproduction and Embryology(ESHRE) consensus meeting guideline
  • include two out of three
  • Oligo - or anovulation
  • Clinical or/and biochemical hyperandrogenism
  • Polycystic ovaries on ultrasound, exclusion of other etiologies( ≥ 12 follicles(2-9 mm diameter) in each ovary or ovarian volume(0.5 x length x width x thickness) ≥ 10cm3)
  • Anatomical normal uterus
  • Normal level of thyroid hormone

Exclusion criteria

  • Severe endometriosis(stageIII, IV)
  • Endometrial thickness less than 7mm in late follicular phase
  • Severe male infertility factor, non-obstructive azoospermia
  • History of ectopic pregnancy or abortion over the last 3 months
  • Unexplained abnormal uterine bleeding
  • Congenital adrenal hyperplasia
  • Androgen secreting tumor
  • Cushing syndrome
  • Concurrent administration of metformin, ovulation induction drugs, oral contraceptives within previous 3 months
  • Chronic disease(liver, kidney, severe heart failure, DM)
  • Any pathology of genital tract
  • History of alcohol abuse
  • Refuse of study participate consent

Treatment and study plan

metformin

Drug

Other names: Glucophage Tab 500mg, National Drug Code(NDC) 0087-6060-05

Primary outcomes

  1. Number of mature(MII) oocyte

    Time frame: Day1(from the day of oocyte retrieval to fertilization confirmation)

    using polarized light microscopy

Secondary outcomes

  1. Clinical pregnancy rate in %

    Time frame: Pregnancy test was carried out at 11 days after embryo transfer and was classified as positive when the serum beta-human chorionic gonadotropin(hCG) level was over 5 IU/L. Than follow up to 12 weeks of gestation.

    Clinical pregnancy was defined as a viable pregnancy beyond 12 weeks gestation by ultrasonographic visualization.

  2. Miscarriage rate in %

    Time frame: Pregnancy test was carried out at 11 days after embryo transfer and was classified as positive when the serum beta-human chorionic gonadotropin(hCG) level was over 5 IU/L. Than follow up to 20 weeks of gestation.

    Miscarriage was defined as a early loss of a pregnancy before 20 weeks of pregnancy.

  3. Total dose of follicle-stimulating hormone(FSH) used(IU)

    Time frame: average of 10 days, From the day of stimulation start with FSH to the day of oocyte retrieval

    compare the ovarian response to controlled ovarian stimulation between two groups

  4. Total duration of FSH used(day)

    Time frame: average of 10 days, From the day of stimulation start with FSH to the day of oocyte retrieval

    compare the ovarian response to controlled ovarian stimulation between two groups

  5. Number of oocytes retrieved

    Time frame: Day1(the day of oocyte retrieval)

    using polarized light microscopy

  6. Number of frozen 2 pronucleus(2PN) embryos

    Time frame: Day1((from the day of oocyte retrieval to fertilization confirmation)

    using polarized light microscopy

  7. Follicular fluid Tumor necrosis factor(TNF)-α level in pg/ml and follicular fluid Adiponectin level in pg/ml and follicular fluid Interleukin-6 level in pg/ml and follicular fluid Anti-mullerian hormone(AMH) level in pg/ml

    Time frame: Day 1

    At the day of oocyte retrieval, follicular fluids were collected from the follicles with a diameter over than 15mm. The fluids were frozen within 4 hours for the future analysis. All the samples were stored at -20℃ and were analysed in the biochemistry department of the study centre.

  8. Serum TNF-α level in pg/ml and serum Adiponectin level in pg/ml and serum Interleukin-6 level in pg/ml and serum AMH level in pg/ml and serum Testosterone level in pg/ml and serum Estradiol level in pg/ml

    Time frame: Day 1

    Serum samples were obtained on the day of Metformin commencement and ovum pick up. Levels are measured by means of solid-phase enzyme-linked immunosorbent assay.

Sponsors and collaborators

Lead sponsor

Chung-Hoon Kim

Other

Registry information

Official study title

A Multicenter, Prospective, Randomized Study to Assess the Effect of Metformin Supplementation on IVF Outcome and Intrafollicular Environment in Patients With Polycystic Ovarian Syndrome Undergoing In Vitro Fertilization/Embryo Transfer

Important dates

Study start
2011
Primary completion
2015
Study completion
2015
First posted
Mar 22, 2017
Registry last updated
May 11, 2017

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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