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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01518829
Other study ID # HCC and Procalcitonin
Secondary ID
Status Completed
Phase N/A
First received January 24, 2012
Last updated September 29, 2013
Start date April 2012
Est. completion date January 2013

Study information

Verified date September 2013
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority Egypt: Institutional Review Board
Study type Observational

Clinical Trial Summary

the value of serum procalcitonin in differentiation between bacterial infection and non infectious inflammation in febrile HCC patients following locoeregional treatment for HCC.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date January 2013
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

1. - Hepatocellular carcinoma patients who will undergo TACE and/or radio-frequency.

2. - Fever more than 38C after 48 hours post intervention.

Exclusion Criteria:

1. HCC Patients who does not develop fever after intervention.

2. Proven infection elsewhere (e.g. UTI, chest infection..)

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Locations

Country Name City State
Egypt Tropical medicine department and hepatocellular carcinoma clinic Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Differantiate between post- embolization syndrom and sepsis following locoregional treatment for hepatocellular carcinoma 6months Yes
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