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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01307163
Other study ID # ran19-HMO-CTIL
Secondary ID esti19
Status Not yet recruiting
Phase N/A
First received January 10, 2008
Last updated March 1, 2011
Start date January 2008
Est. completion date December 2008

Study information

Verified date December 2007
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

Saliva is used nowadays as a significant diagnostic tool due to the latest technological developments. The research compares two experimental groups; children after liver transplantation and a control group.

Our objective is to identify from all the parameters that are evaluated, the ones that differ between the two groups. If such parameters will be found and differ statistically, it will be possible to create a non invasive medical examination protocol, which will probably be much more complaint, and being so would help locate individuals in risk groups with the tendency to develop an end-organ liver disease.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group 2 Years to 16 Years
Eligibility Inclusion Criteria:

- Children after a successful liver transplantation

Study Design

Observational Model: Cohort


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Hadassah Medical Organization IRB Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

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