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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03402165
Other study ID # Alfafetoprotein
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date January 1, 2017
Est. completion date December 30, 2022

Study information

Verified date August 2018
Source Tanta University
Contact Sherief Abd-Elsalam, md
Phone 00201095159522
Email sheriefabdelsalam@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Alpha-fetoprotein Levels on the Response to direct Antiviral Therapy in Patients with Chronic Hepatitis C


Description:

Impact of Serum Alpha-fetoprotein Levels on the Response to direct Antiviral Therapy in Egyptian Patients with Chronic Hepatitis C


Recruitment information / eligibility

Status Recruiting
Enrollment 1200
Est. completion date December 30, 2022
Est. primary completion date December 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- HCV patients who will undergo treatment by direct acting antiviral agents.

Exclusion Criteria:

- Patients with decompensated liver disease

Study Design


Intervention

Drug:
Sofosbuvir and Ledipasvir or sofosbuvir and daklatasuvir
Response to DAAD's and developing HCC

Locations

Country Name City State
Egypt Sherief Abd-Elsalam Tanta

Sponsors (1)

Lead Sponsor Collaborator
Sherief Abd-Elsalam

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with sustained virologic response The total number of patients with SVR in each group 6 months
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