CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 3,434 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01726439
NCT01726439N/ACompleted

A 5-year Prospective and Observational Study to Evaluate the Effectiveness of Nucleos(t)Ide Analogs (NUC) Therapy Among Chronic Hepatitis B (CHB) Patients Naive to NUC in Real World Practice at Hospitals in Tier 2 Cities in China (the EVOLVE Study)

Bristol-Myers Squibb·observational·Posted Nov 15, 2012·Updated Jul 15, 2020

In Brief

An observational study for Chronic Hepatitis B. Completed, enrolled 3,434 participants across 54 sites.

Detailed Summary

To compare the effectiveness, in a real world practice setting in tier 2 cities of China, of Entecavir (ETV) monotherapy and Lamivudine (LAM) based therapies (including LAM monotherapy, de novo LAM + Adefovir \[ADV\] combination, and early add-on of ADV) among chronic hepatitis B (CHB) patients who are naive to NUC at enrollment to this study

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedNov 15, 2012
Enrollment StartDec 1, 2012
Primary CompletionDec 31, 2018
TodayJul 2, 2026
Enrollment to primary: 6.1 yearsPosted 13.6 years ago