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Hepatitis C clinical trials

View clinical trials related to Hepatitis C.

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NCT ID: NCT04525690 Completed - Hepatitis C Clinical Trials

Improving Inpatient Screening for Hepatitis C

Start date: September 21, 2020
Phase: N/A
Study type: Interventional

This study will use a stepped-wedge cluster randomized clinical trial to evaluate a health system initiative to set defaults in the electronic health record admission order set to nudge inpatient hepatitis C (HCV) screening.

NCT ID: NCT04515797 Completed - Hepatitis C Clinical Trials

QUICKly Eradicate Hepatitis C in Patients Undergoing REnal Transplant With 4 Weeks of Glecaprevir/Pibrentasvir

QUICK-CURE
Start date: May 1, 2021
Phase: Phase 4
Study type: Interventional

This is a single center study characterizing the experience of administration of 4 weeks of pan-genotypic DAA therapy in kidney transplantation to prevent the transmission of hepatitis C virus infection from an HCV-positive donor kidney to an HCV-negative recipient.

NCT ID: NCT04513899 Completed - Clinical trials for Hepatitis C Virus (HCV) Infection

Development of a Community-based HCV Treatment Completion Intervention Among HCV Positive Homeless Adults

Start date: October 5, 2020
Phase: N/A
Study type: Interventional

This randomized controlled trial (RCT) will test the efficacy of a Community Health Worker/Registered Nurse (CHW-RN) HCV intervention for homeless individuals, many who are also drug users. The intervention will be designed during Phase I of the proposal using an iterative process between a Community Advisory Board (CAB) and focus groups. The CHW/RN intervention will occur over a 2 or 3 month (8-12 weeks) period depending on the Direct-Acting Antiviral (DAA) prescribed. Homeless adults assigned to the CHW/RN HCV treatment group will receive culturally-sensitive education, case management, and daily DOT delivery of DAA by an RN-guided CHW. The CHW will run a brief (20 min) weekly 1:1 education and 20 min case management session over the 8 or 12 weeks and will deliver all components of the program (which will be developed and refined during Phase I). The CHW-RN HCV intervention will be compared to a clinic-based standard of care group (cbSOC). Primary outcomes are the completion of the Direct-Acting Agent (DAA) treatment (month 2 or 3) and SVR12 Cure (month 5 or 6). Secondary outcomes are improved mental health status, decrease in substance use, and improved access to health care, and shelter stability at month 5 or 6.

NCT ID: NCT04457050 Completed - Hepatitis C Clinical Trials

Effect of Hepatitis C Clearance on Insulin Resistance

Start date: October 30, 2017
Phase: Phase 4
Study type: Interventional

Chronic hepatitis C infection has been linked to insulin resistance, which is the essential component of metabolic syndrome and type 2 diabetes mellitus. Resistin; an adipokine, has been demonstrated to stimulate the secretion of several inflammatory factors known to play a role in the induction of insulin resistance. we investigated the changes in insulin resistance after hepatitis C clearance in the era of direct antivirals.

NCT ID: NCT04437277 Completed - Hepatitis C Clinical Trials

Screening for Chronic Hepatitis C Virus in Hospitalized Patients

DeViCHO
Start date: November 22, 2019
Phase: N/A
Study type: Interventional

Chronic viral hepatitis C is a public health problem and several management recommendations are available. According to the HAS, hepatitis C screening consists of a targeted screening of people at risk of infection by the virus, in particular to drug users, to people from countries with a high prevalence of the virus or who have received care in those countries, people transfused before 1992, or people who have been or have been imprisoned. Our study proposes to evaluate hepatitis C screening in consenting patients hospitalized in Saint Joseph. These previously identified patients with comorbidities will be cared for according to current national practices that reduce HCV morbidity and mortality.

NCT ID: NCT04427202 Completed - HIV Clinical Trials

Ending Transmission of HIV, HCV, and STDs and Overdose in Rural Communities of People Who Inject Drugs (ETHIC)

ETHIC
Start date: August 14, 2020
Phase: N/A
Study type: Interventional

This study will evaluate the referral to harm reduction services (HRS) including syringe services, naloxone overdose prevention, substance use treatment referral, HIV, HCV, and STD testing and referral and linkage to care through capacity building of existing programs through client services data.

NCT ID: NCT04391985 Completed - Clinical trials for Chronic Hepatitis C Virus Infection

Sofosbuvir/Ombitasvir/Paritaprevir/ Ritonavir and Ribavirin for Hepatitis C Virus Genotype 4 Patients

Start date: March 1, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

enrolled participants were treated orally with SOF plus a fixed dose combination of OBV/PTV/r plus RBV.

NCT ID: NCT04389268 Completed - Hepatitis C Clinical Trials

P300 in Early Cognitive Impairment in Hepatitis C Virus

Start date: February 1, 2018
Phase:
Study type: Observational

Approximately 50% of patients with hepatitis C have complaints of fatigue and cognitive deficits even before the development of significant hepatic impairment.

NCT ID: NCT04387539 Completed - Clinical trials for Chronic Hepatitis C Virus Infection

ٍٍSofosbuvir/Simeprevir/Daclatasvir/Ribavirin and HCV Genotype 4-infected Egyptian Experienced Participants

Start date: March 1, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

Experienced participants who had HCV GT4 infection were treated with Sofosbuvir/Simeprevir/Daclatasvir/Ribavirin (SOF/SMV/DCV/RBV)

NCT ID: NCT04387526 Completed - Clinical trials for Chronic Hepatitis C Virus Infection

Sofosbuvir Plus Daclatasvir With or Without Ribavirin and Chronic HCV Genotype (GT) 4

Start date: April 1, 2016
Phase: Phase 2/Phase 3
Study type: Interventional

This study aims to evaluate the efficacy and safety of DCV plus sofosbuvir (SOF) with or without ribavirin (RBV) for treatment of Egyptian participants infected with HCV GT4.