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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00299637
Other study ID # MCA chorioamnionitis HMO-CTIL
Secondary ID
Status Recruiting
Phase Phase 0
First received March 5, 2006
Last updated November 29, 2006
Start date October 2006
Est. completion date December 2007

Study information

Verified date March 2006
Source Hadassah Medical Organization
Contact david mankuta, MD
Email mankuta@yahoo.com
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

This study will try to determine whether fetuses to mothers having clinical chorioamnionitis have changes in blood flow in middle cerebral artery.


Description:

This study will try to determine whether fetuses to mothers having clinical chorioamnionitis have changes in blood flow in middle cerebral artery.

MCA flow parameters will be evaluated during labor of women with and wthout chorioamnionitis


Recruitment information / eligibility

Status Recruiting
Enrollment 34
Est. completion date December 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria:

- women giving birth week 37-42

- healthy

- one fetus

Exclusion Criteria:

- more than one fetus

- IUGR

- illness or damage to fetus

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Haddasah Medical Organization Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

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