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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03169348
Other study ID # HCV
Secondary ID
Status Recruiting
Phase N/A
First received May 25, 2017
Last updated December 6, 2017
Start date November 1, 2017
Est. completion date September 2019

Study information

Verified date December 2017
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Autoimmune thrombocytopenic purpura is an immunological disorder characterized by increased platelet destruction due to presence of anti-platelet antibodies. Hepatitis C virus infection, which is one of the most common chronic viral infections worldwide, may cause secondary chronic immune thrombocytopenic purpura. It seemed to play a pathogenic role in autoimmune thrombocytopenic purpura. Moreover, the successful response (negative hepatitis C virus - ribonucleic acid) to tapered steroids and antiviral therapy was useful to revert thrombocytopenia


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date September 2019
Est. primary completion date June 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Hepatitis C virus infection and thrombocytopenia before treatment

Exclusion Criteria:

- Infection Hepatitis B virus

- Hypersplenism

- Diseases affecting Bone marrow

- Major clotting factors abnormalities eg. Disseminated intravascular coagulopathy, severe Prothrombin deficiency

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
sofosbuvir daclatasvir
oral tablets
Ledipasvir/sofosbuvir
oral tablets

Locations

Country Name City State
Egypt Assiut University Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary the mean difference on the platelet count 6 month
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