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Completed

NCT Number: NCT03088631

Metformin in Intracytoplasmic Sperm Injection Cycles

The relationship between serum progesterone level on the day of human chorionic gonadotropin administration and outcome of in vitro fertilization /intracytoplasmic sperm injection and embryo transfer has been controversial for several decades. some studies presented data against the negative effect of premature luteinization and reported that elevated serum progesterone had no adverse effect on pregnancy rates in fresh embryo-transfer cycles within different ovarian responses. However, most studies have evaluated the association between serum progesterone level and clinical outcome in fresh in vitro fertilization /intracytoplasmic sperm injection cycles and advocated that serum progesterone elevation on the day of human chorionic gonadotropin administration may adversely affect the clinical outcome by jeopardizing endometrial receptivity.

In addition, the underlying mechanism through which premature luteinization influences clinical outcomes is elusive. some proposed that premature luteinization cause impairment of the endometrial receptivity, which may indicate a change in the implantation window, is more likely to be affected than the oocyte.whereas some documented that the compromised quality of oocytes might also be a cause.

The cut-off point of premature luteinization is not well established until now. Premature luteinization has been variously defined based on serum P levels, with thresholds of 0.9-1.5 ng/mL being used.

Previous studies have shown that metformin inhibits the first steps of steroidogenesis dose-dependently reducing granulosa cells progesterone output. Moreover, other authors have recently reported that low dose metformin could improve in vitro fertilization outcome in non poly-cystic ovarian syndrome repeaters. So, considering the safety of this drug before pregnancy, metformin can be given to consenting patients from first ultrasound monitoring until ovulation triggering.

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Key information

Age range

18 year–38 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Women Health Hospital - Assiut university

Asyut, 71111, Egypt

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • First or second trial ICSI cycle.
  • Age: 20 -38 years
  • BMI: patients with BMI ≥ 30 kg/m2 were advised to lose weight for 6 months through lifestyle modifications.
  • AMH ≥1 ng/ml
  • Basal FSH < 10 IU/ml.
  • Normal uterine cavity evidenced by HSG or office hysteroscopy
  • Normal levels of prolactin and TSH before starting COS cycle

Exclusion criteria

  • Patients with recurrent two or more failed intra-cytoplasmic sperm injection cycles.
  • Uterine anomalies or Synechiae.
  • Severe male factor infertility
  • Patients known to have diabetes, renal, liver disease, alcoholism, or drug abuse were excluded
  • Patients who were on metformin treatment were asked to have a one month washout period before study participation.
  • Poor responders

Treatment and study plan

metformin

Drug

will receive metformin (1500 mg/day) starting with the commencement of oral contraceptive pills in the preceding cycle until the day of human chorionic gonadotropin triggering.

Placebo

Other

will receive corn-flour placebo tablets (three tablets daily).

Primary outcomes

  1. Incidence of premature luteinization in both groups

    Time frame: 12 days

    Serum progesterone measurement ≥ 1.5 ng/ml by Mini-vidas assay was used to diagnose cases of premature luteinization.

Secondary outcomes

  1. ongoing pregnancy rate

    Time frame: 12 weeks

    The number of cases with pregnancy more than 12 weeks of gestation divided by the cycles initiated per 100.

  2. Good quality embryo rate

    Time frame: 20 days

    The number of good day 3 embryos per all two-pronuclear embryos.

  3. Progesterone-to-mature oocyte index (PMOI)

    Time frame: 17 days

    calculated by dividing the serum P level (ng/ml) by the number of mature oocytes.

  4. Progesterone/estradiol ratio

    Time frame: 12 days

    calculated as [progesterone (ng/mL) × 1000]/esatradiol (pg/mL)

  5. Implantation rate

    Time frame: 7 weeks

    The number of gestational sacs observed by trans-vaginal ultrasound divided by the number of embryos transferred.

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

Role of Metformin in Prevention of Premature Luteinization in Intracytoplasmic Sperm Injection Cycles

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Mar 23, 2017
Registry last updated
Sep 17, 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.