Clinical Trials Directory

Trials / Completed

CompletedNCT02798315

Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patients With Chronic Hepatitis C - An Observational Study

Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patients With Chronic Hepatitis C -An Observational Study in Kuwait

Status
Completed
Phase
Study type
Observational
Enrollment
40 (actual)
Sponsor
AbbVie · Industry
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

The interferon-free combination regimen of paritaprevir/r - ombitasvir with or without dasabuvir (ABBVIE REGIMEN) ± ribavirin (RBV) for the treatment of chronic hepatitis C (CHC) has been shown to be safe and effective in randomized controlled clinical trials with strict inclusion and exclusion criteria under well controlled conditions. This observational study is the first effectiveness research examining the ABBVIE REGIMEN ± RBV, used according to local label, under real world conditions in Kuwait in a clinical practice patient population.

Conditions

Timeline

Start date
2016-05-25
Primary completion
2017-06-12
Completion
2017-06-12
First posted
2016-06-14
Last updated
2018-12-31
Results posted
2018-12-31

Source: ClinicalTrials.gov record NCT02798315. Inclusion in this directory is not an endorsement.