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Completed

NCT Number: NCT03737253

Hormone Evaluation in Artificial Reproductive Technology

The aim is to be able to predict the hormonal response according to gonadotropin receptor genotype and hormone type used for treatment of women undergoing in vitro fertilization or egg donation.

Outcome will be measured as pregnancy success, live born babies and unwanted side effects.

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Key information

Age range

25 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Poznan University of Medical Sciences, Poznan, Poland

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About this study

Women undergoing in vitro fertilization receive high doses of the gonadotropins follicle stimulating hormone (FSH) and human chorionic gonadotropin (hCG), which is acting as luteinizing hormone (LH) for stimulation of the ovaries in order to obtain a high number of eggs. There are however marked individual differences in the hormonal response, ranging from lack of increased egg maturation to hyper stimulation. The hypothesis is that genetic variants in the gonadotropin receptors (LH and FSH receptors), are influencing the outcome. This assumption is supported by a recent study on more than 600 women undergoing in vitro fertilization, demonstrating that whereas only 10% of women with asparagine in both genes (FSHR N680S and LHR N312S) became pregnant, 40% of those with serine did (Lindgren I et al. Hum Repr 2016; 3:672-83).

Most (90%) of the women were treated with rFSH (recombinant). However, of the 10% asparagine carriers who actually became pregnant, most if not all, were treated with menotropin - a urine derivated compound (Menopur, Ferring), which contains both LH and FSH. This finding was not stressed in the manuscript as it could have been due to chance because of the small number of women treated with menotropin.

The objective is therefore to perform a prospective randomized study regarding efficacy of treatment in the first and second in vitro fertilization trial with rFSH and menotropin, respectively, genotype taken into account.

In total 890 women, 445 in Poznan, Poland and 445 in Malmö, Sweden, with unexplained infertility or a male or tubal factor indication for treatment will be invited to participate in the study. At first appointment, information is provided and informed consent retrieved. Two blood samples are drawn and stored at -20°C; one for subsequent genotyping and one for anti mullerian hormone measurement. The succeeding treatment is according to normal procedures at respective clinic.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Normal ovulatory cycles 26-32 days
  • First and second IVF treatment
  • Indication for IVF is male factor, tubal factor or unexplained infertility
  • Medical indication for IVF; >12 months unprotected intercourse

Exclusion criteria

  • Anti Müllerian Hormone <5pmol or cycle day 2-3 FSH >12
  • Endometriosis
  • polycystic ovarian syndrome
  • pre ovarian failure
  • smoking
  • male age more than 56.

Treatment and study plan

Follitropin alpha

Drug

The objective is to measure the effect of the drug according to gonadotropin receptor genotype.

Other names: Gonal F, Puregon, Urofollitropin

menotropin

Drug

The objective is to measure the effect of the drug according to gonadotropin receptor genotype.

Other names: Menopur

Primary outcomes

  1. Pregnancy

    Time frame: up to 12 months after treatment

    Association between pregnancy rate and genotype is evaluated

Secondary outcomes

  1. Number of oocytes

    Time frame: up to 6 months after treatment

    Number of eggs developed in response to drug according to genotype is measured

  2. live birth

    Time frame: up to 12 months after treatment

    Live birth rate according to genotype is analyzed

Other outcomes

  1. Ovarian hyper stimulation syndrome

    Time frame: Up to 6 months after treatment

    Association between overreaction to hormonal stimulation and genotype is analysed

  2. Poor response

    Time frame: Up to 6 months after treatment

    No or poor development of eggs in response to drug is analysed, genotype taken into account

Sponsors and collaborators

Lead sponsor

Lund University

Other

Collaborators

  • European Commission

Registry information

Official study title

Clinical Study on Pharmacogenetics of Gonadotropin Receptors in Relation to Pregnancy and Life Birth Rate as Well as Unwanted Side Effects Such as Ovarian Hyper Stimulation Syndrome During Assisted Reproduction.

Acronym: HEART

Important dates

Study start
2016
Primary completion
2021
Study completion
2024
First posted
Nov 9, 2018
Registry last updated
Mar 17, 2025

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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