Hyalornic Acid Level in β-Thalassemic Children Treated for Hepatitis C Virus

PHASE4CompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

October 1, 2017

Primary Completion Date

December 31, 2018

Study Completion Date

March 1, 2019

Conditions
Beta-ThalassemiaHepatitis C
Interventions
DRUG

Ledipasvir 90 MG / Sofosbuvir 400 MG [Harvoni]

The fifty (50) thalassemic children infected with HCV received the new direct-acting antiviral therapy in the form of Ledipasvir (90 mg)/Sofosbuvir (400 mg); (Harvoni) as a single oral tablet /day for 12 weeks Follow up of these patients was performed for 24 weeks. Re-evaluation of these children after 24 weeks from initiation of Ledipasvir/Sofosbuvir treatment was performed by repeating clinical assessment, Fibroscan of liver , laboratory investigations including quantitative HCV RNA by PCR and serum hyaluronic acid measurement.

Trial Locations (1)

31527

Pediatric Hematology Unit, Faculty of Medicine, Tanta University, Tanta

All Listed Sponsors
lead

Tanta University

OTHER

NCT03961828 - Hyalornic Acid Level in β-Thalassemic Children Treated for Hepatitis C Virus | Biotech Hunter | Biotech Hunter