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Management of Patients With Hepatitis C in a Public Health Care Setting: The Punjab Model

Efficacy of Decentralized Care in the Management of Patients With Hepatitis C in a Public Health Care Setting: The Punjab Model

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03488485
Enrollment
50000
Registered
2018-04-05
Start date
2016-06-18
Completion date
2020-12-31
Last updated
2019-06-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Hepatitis c

Keywords

Mukh Mantri Punjab Hepatitis C Relief Fund,MMPHCRF, Direct antivirals, DAAs, Chronic hepatitis C

Brief summary

Background and Aims: The prevalence of hepatitis C virus infection (HCV) infection in Punjab, India is 3.29%, with an estimated burden of around 650,000 viremic chronic HCV (CHC) patients. The Mukh Mantri Punjab Hepatitis C Relief Fund (MMPHCRF) was launched in June 2016 to provide free treatment to all CHC aiming to eliminate HCV from Punjab. The study assessed the feasibility of decentralized care and efficacy and safety of 12 or 24 weeks of sofosbuvir (SOF) + ledipasvir (LDV) or SOF + daclatasvir (DCV) ± ribavirin (RBV) in the treatment of CHC patients in a public health care setting.

Detailed description

An algorithm was developed using SOF-based regimens to treat all patients (RKD). Genotyping is not recommended for patients without cirrhosis of liver and they are being treated with SOF+DCV for 12-weeks, while genotyping is recommended for patients with cirrhosis of liver (Figure 1). Patients with liver cirrhosis and genotype 3 are being treated with SOF+DCV+RBV for 24 weeks, while non-genotype 3 patients are being treated with SOF+LDV+RBV for 12-weeks or with SOF+LDV for 24-weeks (in RBV intolerant patients). SVR-12 is mandatory in all patients. Methods: Decentralized care: All patients are being evaluated and treated at 3 Government Medical Colleges and 22 District Hospitals; they were followed up to 12 weeks post-treatment to look for sustained viral response (SVR-12). Health care worker capacity building: 90 medical specialists were trained in a 4-hr predefined course, followed by online continued medical education sessions by regular Extension for Community Healthcare Outcomes (ECHO) Clinic are being conducted fortnightly. 50 pharmacists, 2 from each of the 25 centres, dispense medicine as per specialist prescription. Data Management: 25 trained data entry operators and Clinton Health Access Initiative (CHAI) are managing epidemiological data on CHC hotspots, high-risk groups, local service providers, etc. Monitoring: Medical alerts are being used for compliance monitoring. Study design: A cost-effective algorithm has been developed using SOF-based regimens to treat all patients. The diagnosis of cirrhosis is based on clinical evidence including Aspartate Transaminase (AST)-to-platelet ratio index (APRI ≥ 2.0) and FIB-4 score (\>3.25) or on liver stiffness measurement (LSM) ≥12.5 kilopascal (kPa) on fibroscan. The study aims to validate the efficacy and safety of generic all oral Direct Acting Antiviral (DAA) regimens in a decentralized algorithm based public health model in Punjab, India regardless of genotype/presence of cirrhosis.

Interventions

DAAs given in patients with viremic chronic hepatitis C

Sponsors

Directorate of Health and Family Welfare, Punjab
CollaboratorOTHER
Post Graduate Institute of Medical Education and Research, Chandigarh
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Real Life Efficacy Study

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Chronic Hepatitis C * Age: \>18 years

Exclusion criteria

* Chronic liver disease of a non-HCV etiology * Serum Creatinine \>1.5 mg/dl * Evidence of hepatocellular carcinoma or other malignancy * Significant cardiovascular, pulmonary, or neurological disease * History of solid organ or bone marrow transplantation.

Design outcomes

Primary

MeasureTime frameDescription
Sustained Virological ResponseUp to study completion ( average 12 -24 weeks after therapy)HCV RNA Load undetectable

Secondary

MeasureTime frameDescription
Serious adverse effectsUp to study completion ( average 12 -24 weeks after therapy)Assessment of drug related adverse effects, clinical events, decompensation of liver disease

Countries

India

Contacts

Primary ContactRadha K Dhiman, DM
rkpsdhiman@hotmail.com911722756335

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026