Changes in Blood Flow in MCA of Fetuses to Mothers Having Clinical Chorioamnionitis

NCT ID: NCT00299637

Last Updated: 2006-11-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

34 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-10-31

Study Completion Date

2007-12-31

Brief Summary

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

Detailed Description

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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

Conditions

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Chorioamnionitis

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

OTHER

Eligibility Criteria

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Inclusion Criteria

* women giving birth week 37-42
* healthy
* one fetus

Exclusion Criteria

* more than one fetus
* IUGR
* illness or damage to fetus
Minimum Eligible Age

20 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Hadassah Medical Organization

OTHER

Sponsor Role lead

Principal Investigators

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David Mankuta, MD

Role: STUDY_CHAIR

Hadassah Medical Organization

Locations

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Haddasah Medical Organization

Jerusalem, , Israel

Site Status RECRUITING

Countries

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Israel

Central Contacts

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david mankuta, MD

Role: CONTACT

Email: [email protected]

Facility Contacts

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David Mankuta

Role: primary

Other Identifiers

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MCA chorioamnionitis HMO-CTIL

Identifier Type: -

Identifier Source: org_study_id