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Low Molecular Weight Heparin in Recurrent Implantation Failure

Empirical Low Molecular Weight Heparin Administration in the Luteal Phase in Patients With Recurrent Implantation Failures: a Randomized Open Labeled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00750451
Enrollment
Unknown
Registered
2008-09-10
Start date
2006-01-31
Completion date
2008-05-31
Last updated
2009-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fertilization in Vitro, Infertility, Recurrent Implantation Failure

Keywords

fertilization in vitro, assisted reproduction, recurrent implantation failure, low molecular weight heparin, heparin, luteal phase

Brief summary

Recurrent implantation failure is the failure to achieve a pregnancy after multiple attempts with in vitro fertilization treatment. The reason is usually obscure. Many empirical treatments have been offered without substantial evaluation. Heparin is thought to play a role in the embryo implantation process beyond its anticoagulation effects. The proposed study aims to assess the effectiveness and safety of empirical administration of low molecular weight heparin in patients undergoing a new IVF treatment cycle after multiple failed attempts.

Interventions

DRUGlow molecular weight heparin (enoxaparine sodium)

1 mg/kg/day subcutaneously in the luteal phase after IVF treatment

routine luteal phase support with progesterone gel

Sponsors

V.K.V. American Hospital, Istanbul
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 38 Years
Healthy volunteers
No

Inclusion criteria

* History of at least two previously failed fresh embryo transfer cycles * All previously failed cycles to be performed in the American Hospital of Istanbul * Female age ≤ 38 years * Fresh ejaculate sperms to be used for ICSI * No hormonal, coagulation, or immunological disorders detected * Normal uterine cavity, as assessed by diagnostic office hysteroscopy or saline infusion sonography * Normal female and male peripheral karyotype

Design outcomes

Primary

MeasureTime frame
Ongoing pregnancy beyond the 20th gestational week rate

Secondary

MeasureTime frame
Clinical pregnancy rate
Embryo implantation rate

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026