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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03444272
Other study ID # HCV TREATMENT
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date January 1, 2018
Est. completion date December 2022

Study information

Verified date October 2020
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

Effect of direct-acting antiviral drugs on erectile function


Description:

Effect of direct-acting antiviral drugs on erectile function in HCV patients


Recruitment information / eligibility

Status Recruiting
Enrollment 105
Est. completion date December 2022
Est. primary completion date December 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - HCV infected patients - Male Exclusion Criteria: - HCC - Age below 18 years

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Sofosbuvir and Daklatasuvir
HCV Treatment (Sofosbuvir and Daklatasuvir)

Locations

Country Name City State
Egypt Sherief Abd-Elsalam Tanta

Sponsors (2)

Lead Sponsor Collaborator
Sherief Abd-Elsalam Benha University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with improved erectile functions Number of patients with improved erectile functions 6 months
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