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Clinical Trials/NCT02385461
NCT02385461
Unknown
Not Applicable

A Proposal of a Prospective Study on Prevention of Pregnancy Loss in Women Carrying Inherited Thrombophilia

Casa Sollievo della Sofferenza IRCCS1 site in 1 country108 target enrollmentJanuary 2012

Overview

Phase
Not Applicable
Intervention
Low Molecular Weight Heparins (LMWHs)
Conditions
Pregnancy Complications
Sponsor
Casa Sollievo della Sofferenza IRCCS
Enrollment
108
Locations
1
Primary Endpoint
Number of live births
Last Updated
7 years ago

Overview

Brief Summary

The occurrence of a spontaneous fetal loss (FL) is a rather frequent event: it has been estimated that up to 15% of pregnancies result in a fetal loss. However, recurrent events, defined as >2 or >3 loss, depending on the guidelines used (American College of Obstetricians and Gynecologists or Royal College of Obstetricians Gynaecologists guidelines), occur in 1 % of all pregnancies and it is noteworthy that Recurrent Fetal Loss ( RFL) in about 30-40% of cases remain unexplained after standard gynaecological, hormonal and karyotype investigations. Furthermore, it is important to consider that chromosomal abnormalities are responsible for at least 60% of FL in the first trimester, thus an abnormal karyotype in the fetus should be excluded prior to consider testing women for genetic susceptibility to placental vascular complications (inherited thrombophilia).

Common inherited conditions, the factor V Leiden (FV) and the factor II G20210A (FII) mutations have been recognized as risk factors for FL.

The efficacy of treatment with antithrombotic drugs during pregnancy in women with a history of RFL/ Intra Uterine Fetal Death (IUFD) and thrombophilia is still debated, due to scarcity of available data. Italian guidelines suggest the use of Low-Molecular-Weight Heparin (LMWH) in women with FV or FII mutations and previous otherwise unexplained obstetric complications, while guidelines released by RCOG suggest that heparin therapy during pregnancy may improve the live birth rate in women with second trimester loss associated with inherited thrombophilias. Hence, the idea to propose this prospective observational study comparing clinical data and outcomes in women with common inherited thrombophilias and in women without.

During this study the investigators will collect and evaluate clinical data from examinations and visits by patients, eligible for the study as carriers of thrombophilic defects. This observation will begin before pregnancy and continue until the puerperium, allowing us to study all possible factors influencing these conditions. The study will add knowledge for improving feto-maternal prognosis and preventing spontaneous and recurrent FL.

Plan of the study: multicenter observational study

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
December 2020
Last Updated
7 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Casa Sollievo della Sofferenza IRCCS
Responsible Party
Principal Investigator
Principal Investigator

Elvira Grandone, MD, Head of Unit

A proposal of a prospective study on prevention of pregnancy loss in women carrying inherited thrombophilia.

Casa Sollievo della Sofferenza IRCCS

Eligibility Criteria

Inclusion Criteria

  • recurrent otherwise unexplained FL (defined as \>3, or 2 in the presence of at least 1 normal fetal karyotype) (according to Lussana et al.) or
  • at least 1 intrauterine fetal death (IUFD), defined as a loss after 20 weeks of a morphologically normal fetus with/without HETEROZYGOUS FOR FACTOR V LEIDEN or HETEROZYGOUS FOR FIIA20210 (PTm)

Exclusion Criteria

  • personal history of venous and/or arterial thromboembolism;
  • documented hemorrhagic disease;
  • allergy to LMWH;
  • uterine abnormalities;
  • cervical incompetence;
  • untreated endocrine diseases (diabetes mellitus or thyroid disease);
  • indication to anticoagulant treatment during pregnancy;
  • chromosomal abnormalities in parents

Arms & Interventions

Inherited Thrombophilia

Women with Common Inherited Thrombophilias and previous foetal loss

Intervention: Low Molecular Weight Heparins (LMWHs)

Other Thrombophilias with Pregnancy loss

Women with Thrombophilias other than common inherited thrombophilias and previous foetal loss

Intervention: Low Molecular Weight Heparins (LMWHs)

No thrombophilia

Women without thrombophilias and previous foetal loss

Intervention: Low Molecular Weight Heparins (LMWHs)

Outcomes

Primary Outcomes

Number of live births

Time Frame: 10 months

Study Sites (1)

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