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Role of Heparin in Poor Responders Undergoing In Vitro Fertilisation

N

National and Kapodistrian University of Athens

Status and phase

Completed
Phase 3
Phase 2

Conditions

Infertility

Treatments

Drug: no heparin
Drug: Heparin, Low-Molecular-Weight

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The addition of heparin increases pregnancy outcome parameters in poor responders undergoing In Vitro Fertilisation (IVF)

Enrollment

50 patients

Sex

Female

Ages

25 to 43 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • poor responders (age>40, abnormal ovarian test, </=4 oocytes in previous cycle with conventional stimulation)
  • infertility, indication for IVF
  • no contraindications for heparin

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

Heparin, Low-Molecular-Weight group
Experimental group
Description:
LMWH was administered during an IVF cycle using either the GnRH - agonist or antagonist protocol in poor responders. Drug was started at the beginning of the cycle and stopped at the time of pregnancy test if negative, or continued if pregnancy occurred until the 32th weeks of gestation
Treatment:
Drug: Heparin, Low-Molecular-Weight
Non Heparin, Low-Molecular-Weight group
Active Comparator group
Description:
IVF cycle using either the GnRH - agonist or antagonist protocol in poor responders.
Treatment:
Drug: no heparin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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