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Completed

NCT Number: NCT02607319

Low Molecular Weight Heparin to Improve Pregnancy Outcome in Patients With Recurrent Implantation Failure

The objective of this study is to determine the effect of Bemiparin, a low molecular weight heparin, on implantation rate in women with unexplained recurrent implantation failure undergoing IVF/ICSI treatment.

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Key information

Age range

18 year–38 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

American University of Beirut Medical Center

Beirut, Lebanon

About this study

Recurrent implantation failure (RIF), defined as failure of conception following three or more consecutive In Vitro Fertilization (IVF) cycles despite the transfer of good quality embryos, is a major cause of distress amongst infertile couples. While factors underlying implantation failure are many, most cases remain unexplained. In order to improve pregnancy outcomes and delivery rates in women with unexplained RIF, various investigational treatments have been proposed.

The investigators propose a prospective controlled randomized comparative study to evaluate the effect of Bemiparin on implantation rates in women with unexplained RIF. A total of 200 patients will be recruited and randomized between two groups. The study group will receive Bemiparin plus standard care; while the control group will receive only standard care. Treatment will start on the day following embryo transfer and will be continued until 12 weeks gestation in the event of pregnancy.

The primary objective is to determine the effect of Bemiparin on implantation rate in women with unexplained recurrent implantation failure.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • History of three or more consecutively failed In Vitro Fertilization (IVF) cycles after embryo transfer.
  • Normal uterine cavity (as assessed by hysteroscopy or HSG).
  • Normal hormonal investigation: TSH, PRL, FBS.
  • Normal acquired/inherited thrombophilia profile: LAC, ACA IgG/IgM, Prot S, Antithrombin III, beta-2 glycoprotein, Factors V, II, MTHFR.
  • Normal semen analysis and mild/moderate male factor (Total motile sperm count > 5 million/ml and/or normal WHO morphology >20%.
  • Patient provides written informed consent.

Exclusion criteria

  • Evidence of low ovarian reserve by at least one of the following: AMH ≤ 1,5 ng/mL and/or basal CD 3 FSH ≥ 10 mIU/mL and/or basal CD 3 Estradiol ≥ 60 ng/mL and/or previous egg collection yield ≤ 3 oocytes.
  • Preexisting medical condition (thyroid disease, diabetes mellitus, hypertension, pulmonary conditions, cardiac condition…).
  • Severe male factor infertility (Total motile sperm count < 5 million/ml and/or normal WHO morphology <20%).
  • Hypersensitivity to Heparin or its derivatives.
  • Acquired thrombophilia.
  • Active hemorrhage or increased risk of bleeding due to impairment of homeostasis.
  • Severe impairment of liver or pancreatic function.
  • Severe renal insufficiency (Creatinine Clearance < 30 ml/min).
  • Injuries to or operations on the central nervous system, eyes and ears within the last 2 months.
  • Disseminated Intravascular Coagulation (DIC) attributable to heparin-induced thrombocytopenia.
  • Acute bacterial endocarditis and endocarditis lenta.
  • Any organic lesion with high risk of bleeding (e.g.: active peptic ulcer, hemorrhagic stroke, cerebral aneurysm or cerebral neoplasms).

Treatment and study plan

Bemiparin sodium

Drug

Bemiparin sodium 3,500 IU will be started on the evening of the same day of embryo transfer and until the day of pregnancy test. If the test is positive, Bemiparin will be discontinued by the end of the 12th week of gestation.

Other names: Hibor

Primary outcomes

  1. Implantation rate (%)

    Time frame: Vaginal ultrasound at 8 weeks gestation

    Number of intrauterine gestational sacs observed by transvaginal ultrasonography divided by the number of transferred embryos

Secondary outcomes

  1. Live birth rate (%)

    Time frame: Time of delivery up to 42 weeks gestation

    birth of live born

  2. Ongoing pregnancy rate (%)

    Time frame: Vaginal ultrasound at 20 weeks of gestation

    Fetal heart beat seen by ultrasound at 20 weeks gestation

  3. Clinical pregnancy rate (%)

    Time frame: Vaginal ultrasound at 8 weeks gestation

    Fetal heart beat seen by ultrasound at 8 weeks gestation

  4. Total pregnancy rate (%)

    Time frame: Up to 15 days from oocyte collection

    Positive hCG titer

Sponsors and collaborators

Lead sponsor

American University of Beirut Medical Center

Other

Registry information

Official study title

Effect of Low Molecular Weight Heparin (Bemiparin) on Implantation Rate in Patients With Recurrent Implantation Failure Undergoing IVF/ICSI - A Prospective Randomized Clinical Trial

Acronym: BRIF

Important dates

Study start
2015
Primary completion
2022
Study completion
2022
First posted
Nov 18, 2015
Registry last updated
Jul 20, 2023

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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