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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01548820
Other study ID # HBV resistance
Secondary ID
Status Completed
Phase N/A
First received March 6, 2012
Last updated September 8, 2013
Start date June 2010
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

On treatment parameters for Lamivudine resistance in HBV treated Egyptian patients


Description:

Primarily: To study the correlations between the following parameters in adult Egyptian patients with chronic viral hepatitis B before treatment:

- ALT.

- HBeAg.

- HBV-DNA by quantitative PCR.

- Biopsy (if possible). Secondarily: After receiving lamivudine therapy we will identify the impact of these parameters on viral breakthrough at 1 year of therapy.


Recruitment information / eligibility

Status Completed
Enrollment 230
Est. completion date January 2013
Est. primary completion date November 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Adult patients >18 years old

- Egyptian nationality

- Positive serology for HBsAg for more than 6 months

- Positive HBV viremia (above 2000IU/ml).

- Lamivudine monotherapy

Exclusion Criteria:

- Anti-HBcIgM seropositivity

- Positive serology for HCV

- Positive serology for HDV

- Patients complicated with HCC

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Locations

Country Name City State
Egypt Tropical medicine department 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 Resistance to Lamivudine Therapy Prevelance of Lamivudine resistance among HBV Egyptian cases pretreatment and on treatment parameters for Lamivudine therapy resistance 1 year No