PAR Family Polymorphisms and Placental Invasion Disorders

NCT00425867 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2007-01-26

No results posted yet for this study

Summary

The present study will be undertaken to establish whether genetic variations of PAR1 could be involved in the occurrence of any of the "placental syndromes" of preterm delivery, preeclampsia, and/or small for gestational age babies and recurrent pregnancy loss.

Conditions

  • Miscarriage, Recurrent
  • Premature Labor

Interventions

BEHAVIORAL

PAR1 polymoprhisms and placental invasion

Sponsors & Collaborators

  • Shaare Zedek Medical Center

    lead OTHER

Principal Investigators

  • Sorina Grisaru, MD · Shaare Zedek Medical Center

Eligibility

Min Age
20 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-03-31
Completion
2007-11-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00425867 on ClinicalTrials.gov