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The Role of Pro-angiogenic Immune Cells in Human Pregnancies

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ClinicalTrials.gov Identifier: NCT01177020
Recruitment Status : Unknown
Verified August 2010 by Hillel Yaffe Medical Center.
Recruitment status was:  Recruiting
First Posted : August 6, 2010
Last Update Posted : August 6, 2010
Sponsor:
Information provided by:

Study Description
Brief Summary:
Identification of the presence of proangiogenic immune cells in normal human placentas may enable predication of some pregnancy disorders.

Condition or disease Intervention/treatment
Fetal Growth Retardation Preeclampsia Other: Biological specimen

Study Design

Study Type : Observational
Estimated Enrollment : 300 participants
Observational Model: Case Control
Time Perspective: Retrospective
Study Start Date : August 2010
Estimated Primary Completion Date : August 2011
Estimated Study Completion Date : December 2011

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Groups and Cohorts

Group/Cohort Intervention/treatment
Placentas after delivery or abortion Other: Biological specimen
Biological specimen taken from placenta


Outcome Measures

Primary Outcome Measures :
  1. To find the angiogenic potential of proangiogenic immune cells derived from human placentas. [ Time Frame: Two years ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Placentas after delivery or abortion
Criteria

Inclusion Criteria:

  • Placentas that have been delivered in the Medical Center

Exclusion Criteria:

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): NCT01177020


Contacts
Contact: Elad Mei-Dan, MD 972-4-6304248 eladmei@yahoo.com

Locations
Israel
Hillel Yaffe Medical Center Recruiting
Hadera, Israel, 38100
Principal Investigator: Elad Meidan, MD         
Sponsors and Collaborators
Hillel Yaffe Medical Center
More Information

Responsible Party: Elad Mei-Dan, MD, Hillel Yaffe Medical Center
ClinicalTrials.gov Identifier: NCT01177020     History of Changes
Other Study ID Numbers: HYMC1069A
First Posted: August 6, 2010    Key Record Dates
Last Update Posted: August 6, 2010
Last Verified: August 2010

Additional relevant MeSH terms:
Pre-Eclampsia
Fetal Growth Retardation
Hypertension, Pregnancy-Induced
Pregnancy Complications
Fetal Diseases
Growth Disorders
Pathologic Processes