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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03770936
Other study ID # liver fibrosis
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date October 1, 2018
Est. completion date November 2027

Study information

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

Clinical Trial Summary

Effect of Some Drugs on Liver Fibrosis


Description:

The study aimed at evaluating the effect of Some Drugs on Liver Fibrosis


Recruitment information / eligibility

Status Recruiting
Enrollment 45
Est. completion date November 2027
Est. primary completion date October 2026
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- chronic hepatitis C

Exclusion Criteria:

- Acute hepatitis

- Thalassemia

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Candesartan
Candesartan 8 mg/day
Ramipril
ramipril 1.25 mg/day

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 Change in Fibroscan or APRI score Change in Fibroscan or APRI score 6 months
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