Evidence map›Paper›PMID 32356185›Full record

Trial reportArchives of virology2020

High success rates for the use of sofosbuvir/ombitasvir/paritaprevir/ritonavir + ribavirin and sofosbuvir/simeprevir/daclatasvir + ribavirin in retreatment of chronic hepatitis C infection after unsuccessful sofosbuvir/daclatasvir therapy: a real-life experience.

Ebada Mohamed Said, Badawy A Abdulaziz, Mohamed El Kassas, Ibrahim Hussein El Attar, Mohammed Emadeldeen, Sherief M Abd-Elsalam

Retracted Registry-linked trialAbstract readClinical TrialObservational StudyRetracted Publication
PubMed Publisher
In one paragraph

Trial report in Archives of virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. It is linked to trial NCT02992457 (Study of the Safety and Efficacy of Sofosbuvir-Based Regimens in the Treatment of Egyptian Patients With and Without Post-hepatitis C Cirrhosis), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02992457 phase4completednot on this map

Study of the Safety and Efficacy of Sofosbuvir-Based Regimens in the Treatment of Egyptian Patients With and Without Post-hepatitis C Cirrhosis

TypeinterventionalSponsorTanta UniversityRan2015 to 2019Enrolled10,000ConditionsHepatitis CArmsSofosbuvir, Ribavirin, Pegylated-interferon alfa-2a, Simeprevir, Daclatasvir
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Ebada Mohamed SaidHepatology, Gastroenterology and Infectious Diseases Department, Faculty of Medicine, Benha University, Benha, Egypt.
Badawy A AbdulazizHepatology, Gastroenterology and Infectious Diseases Department, Faculty of Medicine, Benha University, Benha, Egypt.
Mohamed El KassasEndemic Medicine Department, Faculty of Medicine, Helwan University, Cairo, Egypt.
Ibrahim Hussein El AttarHepatology, Gastroenterology and Infectious Diseases Department, Faculty of Medicine, Benha University, Benha, Egypt.
Mohammed EmadeldeenNational Hepatology and Tropical Medicine Research Institute (NHTMRI), Cairo, Egypt.
Sherief M Abd-ElsalamTropical Medicine Department, Tanta University, Tanta, Egypt. sherif.abdelbaky@med.tanta.edu.eg.ORCID http://orcid.org/0000-0003-4366-2218
Benha University · EGHelwan University · EGNational Water Research Center · EGTanta University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this work was assessment of the efficacy and tolerability of two different regimens for retreatment of hepatitis C virus (HCV) patients who failed to respond to SOF/DCV-based therapy. This prospective study included 104 HCV patients who failed to respond to SOF/DCV-based therapy. Patients were randomly allocated to two groups. Efficacy and tolerability were assessed. The 12-week sustained virological response (SVR12) rates were 96% and 94.4% in groups B and A, respectively, with no significant difference (p = 1.000). Most adverse events reported were mild to moderate, with no deaths during the study. Multi-target direct-acting antiviral (DAA) combinations are efficient for retreatment of HCV patients after failure of SOF/DCV-based therapy in real-world management.ClinicalTrials.gov identifier: NCT02992457.

Indexed as

AdultAnilidesAntiviral AgentsCarbamatesCyclopropanesDrug Therapy, CombinationFemaleHepatitis C, ChronicHumansImidazolesLactams, MacrocyclicMacrocyclic CompoundsMaleMiddle AgedProlineProspective StudiesAnilidesAntiviral AgentsCarbamatesCyclopropanesdaclatasvirImidazolesLactams, MacrocyclicMacrocyclic CompoundsombitasvirparitaprevirProlinePyrrolidinesRibavirinRitonavirSimeprevirSofosbuvirSulfonamidesValine

Identifiers

PMID32356185
OpenAlexW3023079506

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.