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

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified March 2006 by Hadassah Medical Organization.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00299637
First Posted: March 7, 2006
Last Update Posted: November 30, 2006
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Hadassah Medical Organization
  Purpose
This study will try to determine whether fetuses to mothers having clinical chorioamnionitis have changes in blood flow in middle cerebral artery.

Condition Phase
Chorioamnionitis Early Phase 1

Study Type: Observational
Study Design: Observational Model: Case Control
Observational Model: Natural History
Time Perspective: Cross-Sectional
Time Perspective: Prospective
Official Title: Changes in Blood Flow in MCA of Fetuses to Mothers Having Clinical Chorioamnionitis During Labor Comparing to Fetuses to Healthy Mothers.

Resource links provided by NLM:


Further study details as provided by Hadassah Medical Organization:

Estimated Enrollment: 34
Study Start Date: October 2006
Estimated Study Completion Date: December 2007
Detailed 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

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • more than one fetus
  • IUGR
  • illness or damage to fetus
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00299637


Contacts
Contact: david mankuta, MD mankuta@yahoo.com

Locations
Israel
Haddasah Medical Organization Recruiting
Jerusalem, Israel, 12000
Contact: David Mankuta         
Principal Investigator: David Mankuta         
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Study Chair: David Mankuta, MD Hadassah Medical Organization
  More Information

ClinicalTrials.gov Identifier: NCT00299637     History of Changes
Other Study ID Numbers: MCA chorioamnionitis HMO-CTIL
First Submitted: March 5, 2006
First Posted: March 7, 2006
Last Update Posted: November 30, 2006
Last Verified: March 2006

Additional relevant MeSH terms:
Chorioamnionitis
Fetal Diseases
Pregnancy Complications
Fetal Membranes, Premature Rupture
Obstetric Labor Complications
Placenta Diseases