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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01177020
Other study ID # HYMC1069A
Secondary ID
Status Recruiting
Phase N/A
First received May 12, 2010
Last updated August 5, 2010
Start date August 2010
Est. completion date December 2011

Study information

Verified date August 2010
Source Hillel Yaffe Medical Center
Contact Elad Mei-Dan, MD
Phone 972-4-6304248
Email eladmei@yahoo.com
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Identification of the presence of proangiogenic immune cells in normal human placentas may enable predication of some pregnancy disorders.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date December 2011
Est. primary completion date August 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Placentas that have been delivered in the Medical Center

Exclusion Criteria:

Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Other:
Biological specimen
Biological specimen taken from placenta

Locations

Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary To find the angiogenic potential of proangiogenic immune cells derived from human placentas. Two years No
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