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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00294983
Other study ID # SHEBA-05-3912-JZ-CTIL
Secondary ID
Status Withdrawn
Phase N/A
First received February 19, 2006
Last updated January 28, 2008

Study information

Verified date January 2008
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

Estimating the prevalence of OCD symptoms among patients with burns


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients with burns for at least 6 months and are under treatment

Exclusion Criteria:

- Was not defined

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Chaim Sheba Medical Center Ramat-Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

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