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NCT00458666 Clinical Trial

Coagulation Parameters During Pregnancy in Amniotic Fluid

Pregnancy Clinical Trial

Official title:
Coagulation Parameters During Pregnancy in Amniotic Fluid

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00458666
Other study ID # CoagulationAmnioticFluid_CTIL
Secondary ID
Status Recruiting
Phase N/A
First received April 10, 2007
Last updated April 10, 2007
Start date June 2006

Study information
Verified date March 2007
Source Rambam Health Care Campus
Contact Galit Sarig, Ph.D
Phone +972-50-2061462
Email g_sarig@rambam.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Amniotic fluid embolism is a rare devastating thromboembolic event, which is probably caused by the entrance of amniotic fluid (AF) to the maternal circulation. While AF contains coagulation activators, their role during pregnancy has not been elucidated. The current study aimed to evaluate coagulation parameters in AF during human pregnancy.

Description:

Amniotic fluid embolism is a rare devastating thromboembolic event, which is probably caused by the entrance of amniotic fluid (AF) to the maternal circulation. While AF contains coagulation activators, their role during pregnancy has not been elucidated. The current study aimed to evaluate coagulation parameters in AF during human pregnancy.

Recruitment information / eligibility
Status Recruiting
Enrollment 170
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Women undergoing amniocentesis during 15-35 weeks of gestation.

Exclusion Criteria:

- A history of venous thromboembolism

- Systemic disease i.e.; diabetes, hypertension, hypo or hyper-thyroidism,

- Anticoagulant treatment

- Abnormal embryo

Study Design

Time Perspective: Longitudinal

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Dept of Obstetrics and Gynecology, Rambam-Health Care Campus Haifa

Sponsors (1)
Lead Sponsor Collaborator
Rambam Health Care Campus

Country where clinical trial is conducted

Israel, 

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