Analysis of the duration of combination therapy that is necessary for hepatitis C (HCV) genotype 1 eradication

ISRCTN ISRCTN56141572
DOI https://doi.org/10.1186/ISRCTN56141572
Protocol serial number N0263132921
Sponsor Department of Health
Funder University College London Hospitals NHS Trust (UK)
Submission date
30/09/2004
Registration date
30/09/2004
Last edited
18/07/2016
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Infections and Infestations
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Not provided at time of registration

Contact information

Dr N V Naoumov
Scientific

General Medicine (Hepatology)
Institute of Hepatology
University College London
69-75 Chenies Mews
London
WC1E 6HX
United Kingdom

Phone +44 (0)20 7388 2013
Email n.naoumov@ucl.ac.uk

Study information

Primary study designInterventional
Study designRandomised controlled trial
Secondary study designRandomised controlled trial
Study type Participant information sheet
Scientific titleAnalysis of the duration of combination therapy that is necessary for hepatitis C (HCV) genotype 1 eradication
Study objectivesWhat is the duration of combination therapy required in order to produce a sustained viral clearance in hepatitis C infected patients
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedInfections and Infestations: Hepatitis C
InterventionRandomised Controlled Trial
1. Chemotherapy 1
2. Chemotherapy 2
Intervention typeDrug
PhaseNot Applicable
Drug / device / biological / vaccine name(s)
Primary outcome measure(s)

Viral clearance

Key secondary outcome measure(s)

Not provided at time of registration

Completion date01/10/2005

Eligibility

Participant type(s)Patient
Age groupNot Specified
SexAll
Target sample size at registration50
Key inclusion criteria50 patients from Hepatology
Key exclusion criteriaDoes not match inclusion criteria
Date of first enrolment01/10/2003
Date of final enrolment01/10/2005

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

University College London
London
WC1E 6HX
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Participant information sheet Participant information sheet 11/11/2025 11/11/2025 No Yes

Editorial Notes

18/07/2016: No publications found, verifying study status with principal investigator.