Thromboelastography During and After Delivery

NCT01506102 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2012-01-09

No results posted yet for this study

Summary

The purpose of this study is to establish reference values for thromboelastography (TEM-A) in healthy pregnant women during labor and 2 hours and 24 hours after delivery.

Conditions

  • Delivery Uterine

Interventions

DEVICE

Thromboelastography

Thromboelastography during labor and after delivery

Sponsors & Collaborators

  • Città di Roma Hospital

    lead OTHER

Principal Investigators

  • Silvia Stirparo, MD · Città di Roma Hospital

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-11-30
Primary Completion
2012-05-31
Completion
2012-05-31

Countries

  • Italy

Study Locations

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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 NCT01506102 on ClinicalTrials.gov