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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03646396
Other study ID # sofosbuvir angiogenesis
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2018
Est. completion date December 2025

Study information

Verified date August 2018
Source Tanta University
Contact Sherief Abd-Elsalam, MD
Phone 00201147773440
Email sheriefabdelsalam@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aimed at study of the Effect of Daclatasvir Plus Sofosbuvir on Angiogenesis in Egyptian Patients With Chronic HCV Infection


Description:

The study primary aim was at evaluation of the Effect of Daclatasvir Plus Sofosbuvir on Angiogenesis in Egyptian Patients With Chronic HCV Infection


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 2025
Est. primary completion date August 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Chronic HCV patients

Exclusion Criteria:

- HCC.

- HIV or HBV.

- Malignancy.

- Pregnancy.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Sofosbuvir-daclatasvir
Sofosbuvir-daclatasvir for 3 months

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 change in VEGF, TGFB1 Number of patients with change in VEGF, TGFB1 6 months
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