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Hormone Evaluation in Artificial Reproductive Technology (HEART)

Primary Purpose

Female Infertility

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Follitropin alpha
Menotropin
Sponsored by
Lund University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Female Infertility focused on measuring gonadotropin, receptor, assisted reproduction

Eligibility Criteria

25 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

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.

Sites / Locations

  • Poznan University of Medical Sciences
  • Reproductive Medicine Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Follitropin alpha

Menotropin

Arm Description

Follitropin alpha (GONAL-f, Merck-Serono, Darmstadt, Germany), injections, dosage varying 1500-2500 IU, duration 2-5 days.

Menotropin (Menopur, Ferring GmbH, Kiel, Germany), injections, dosage varying 1500-2500 IU, duration 2-5 days.

Outcomes

Primary Outcome Measures

Pregnancy
Association between pregnancy rate and genotype is evaluated

Secondary Outcome Measures

Number of oocytes
Number of eggs developed in response to drug according to genotype is measured
live birth
Live birth rate according to genotype is analyzed

Full Information

First Posted
October 23, 2018
Last Updated
April 21, 2022
Sponsor
Lund University
Collaborators
Ferring Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT03737253
Brief Title
Hormone Evaluation in Artificial Reproductive Technology
Acronym
HEART
Official Title
Prospective Randomised 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.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
September 1, 2016 (Actual)
Primary Completion Date
December 31, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lund University
Collaborators
Ferring Pharmaceuticals

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Female Infertility
Keywords
gonadotropin, receptor, assisted reproduction

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Women undergoing in vitro fertilization are randomized to either menotropin (urin derivate) or recombinant follicle stimulating hormone. Inclusion criteria are: younger than 40 years of age more than 12 months of unprotected intercourse normal ovulatory cycles 26-32 days first or second IVF treatment indication for IVF is male factor tubal factor or unexplained infertility. Exclusion criteria are: Anti müllerian hormone less than 5pmol or FSH more than 12 cycle day 2-3 Endometriosis polycystic ovarian syndrome pre ovarian failure smoking male age more than 56. The succeeding treatment is according to normal procedures at respective clinic. End points are: total hormonal dosage, number of retrieved oocytes, fertilization rate, rate of blastocyst transfer, pregnancy rate, live birth rate. Adverse effects e.g overstimulation is recorded.
Masking
InvestigatorOutcomes Assessor
Masking Description
Patients and care providers need to know the type of hormone provided in order to be able to instruct and treat the patient. However, all roles are masked regarding the genotype.
Allocation
Randomized
Enrollment
796 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Follitropin alpha
Arm Type
Active Comparator
Arm Description
Follitropin alpha (GONAL-f, Merck-Serono, Darmstadt, Germany), injections, dosage varying 1500-2500 IU, duration 2-5 days.
Arm Title
Menotropin
Arm Type
Active Comparator
Arm Description
Menotropin (Menopur, Ferring GmbH, Kiel, Germany), injections, dosage varying 1500-2500 IU, duration 2-5 days.
Intervention Type
Drug
Intervention Name(s)
Follitropin alpha
Other Intervention Name(s)
Gonal F, Puregon, Urofollitropin
Intervention Description
The objective is to measure the effect of the drug according to gonadotropin receptor genotype.
Intervention Type
Drug
Intervention Name(s)
Menotropin
Other Intervention Name(s)
Menopur
Intervention Description
The objective is to measure the effect of the drug according to gonadotropin receptor genotype.
Primary Outcome Measure Information:
Title
Pregnancy
Description
Association between pregnancy rate and genotype is evaluated
Time Frame
up to 12 months after treatment
Secondary Outcome Measure Information:
Title
Number of oocytes
Description
Number of eggs developed in response to drug according to genotype is measured
Time Frame
up to 6 months after treatment
Title
live birth
Description
Live birth rate according to genotype is analyzed
Time Frame
up to 12 months after treatment
Other Pre-specified Outcome Measures:
Title
Ovarian hyper stimulation syndrome
Description
Association between overreaction to hormonal stimulation and genotype is analysed
Time Frame
Up to 6 months after treatment
Title
Poor response
Description
No or poor development of eggs in response to drug is analysed, genotype taken into account
Time Frame
Up to 6 months after treatment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yvonne Lundberg Giwercman, PhD
Organizational Affiliation
Lund University, Lund, Sweden
Official's Role
Principal Investigator
Facility Information:
Facility Name
Poznan University of Medical Sciences
City
Poznań
Country
Poland
Facility Name
Reproductive Medicine Center
City
Malmö
ZIP/Postal Code
21428
Country
Sweden

12. IPD Sharing Statement

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Hormone Evaluation in Artificial Reproductive Technology

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