Prevalence of Kidney Injury in Patients With HCV Treated With Sofuspovir Containing DAA Therapy

Sponsor
Cairo University (Other)
Overall Status
Unknown status
CT.gov ID
NCT04267458
Collaborator
(none)
300
1
1
18
16.7

Study Details

Study Description

Brief Summary

this study aims is to investigate the occurrence of AKI during antiviral therapy, defined as an increase of 0.3 mg/dL or 50% at least in serum creatinine level when compared with baseline values or more than a 25% reduction in (eGFR) when compared with baseline eGFR in Egyptian patients.In addition to evaluate the change in insulin resistance value after treating patients from HCV.

Condition or Disease Intervention/Treatment Phase
  • Other: evaluation of sofuspovir containing DAA regien expected insult on kidney
Phase 4

Detailed Description

There are limited published data, currently, suggesting the risk of AKI during oral direct acting antiviral treatment. Most case reports and retrospective studies reported the presence of an intrinsic cause of renal injury, with most of the available biopsies showing acute tubular necrosis (ATN) and acute interstitial nephritis (AIN). Most of these patients had returned to baseline renal function on cessation of sofosbuvir combination therapy.

Recently it was found that a notable percentage of patients experienced a transient increase in creatinine during therapy, which could occasionally lead to a more than 50% decrease in patients' eGFR. Previous studies had also shown that the co-use of nonsteroidal anti-inflammatory drugs (NSAIDs) and recurrent ascites were at increased risk for AKI during sofosbuvir-based antiviral therapy.

The primary endpoint of this study is to investigate the occurrence of AKI in Egyptian patients during antiviral therapy and to highlight its reasons and time of incidence in addition to the mechanism of this injury.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
the Prevalence of Acute Kidney Injury in Patients With Chronic Hepatitis c Virus Receiving Sofuspovir Containing Direct Acting Antiviral Therapy
Actual Study Start Date :
Jul 1, 2019
Anticipated Primary Completion Date :
Apr 30, 2020
Anticipated Study Completion Date :
Dec 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Other: HCV infected patients with non-elevated sCr than basal levels

a group of egyption patients with HCV infection with non-elevated sCr than basal levels and treated with sofuspovir as an direct acting antiviral drug

Other: evaluation of sofuspovir containing DAA regien expected insult on kidney
to use different kidney biomarkers to evaluate acute kidney damage after using sofuspovir containing DAA regimen in treatment of HCV

Outcome Measures

Primary Outcome Measures

  1. investigate the renal injury which can be caused during using sofuspovir containing DAA regimen in HCV treatment [from the start to 6 months later]

    to investigate effect of DAA on kidney of treated patients and the mechanism of the drug to cause this renal effect by causing renal buimarkers including NAG and eGFR

Secondary Outcome Measures

  1. highlight the effect of DAAs on insulin resistance in diabetic patients suffering from HCV [from the starting of treatment till the 3-months follow up after the end of the treatment regimen]

    to estimate the effect of DAAs on HOMA-IR index f insulin resistance in diabetic infected patients and comparing their insulin resistance before and after treatment

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients suffering from HCV

  • male or female

  • easy to treat naive patients

Exclusion Criteria:
  • pregnant women

  • seffering from HBV

  • diffecult to treat

  • other comorbodities as heart diseases or COPD

Contacts and Locations

Locations

Site City State Country Postal Code
1 Thabet Thabet Hospital For Internal Diseases Cairo Egypt 11311

Sponsors and Collaborators

  • Cairo University

Investigators

  • Principal Investigator: Dalia Zaafar, PhD, Lecturer of pharmacology and toxicology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dalia K. Zaafar, lecturer of pharmacology, Cairo University
ClinicalTrials.gov Identifier:
NCT04267458
Other Study ID Numbers:
  • 15-2019
First Posted:
Feb 12, 2020
Last Update Posted:
Feb 12, 2020
Last Verified:
Feb 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Dalia K. Zaafar, lecturer of pharmacology, Cairo University

Study Results

No Results Posted as of Feb 12, 2020