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Epidemiological Study to Evaluate Personality Disorders in Prison Populations in Treatment for Hepatitis C

Prospective Observational Study to Assess Personality Disorders in Prison Populations for Hepatitis C Treatment.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01900886
Acronym
Perseo
Enrollment
263
Registered
2013-07-17
Start date
2010-12-31
Completion date
2013-12-31
Last updated
2013-07-17

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

Conditions

Hepatitis C, Chronic, Personality Disorders in Prison

Keywords

prison, disorder, hepatitis c

Brief summary

Primary objective: Evaluate the prevalence of personality disorders in patients starting treatment for hepatitis C in the prison and determine their influence on the evolution of the disease.

Detailed description

Secondary objectives: * Describe the management of patients with personality disorders on treatment for hepatitis C in the prison. * Describe the characteristics of patients who discontinue the treatment and the reasons for stratifying by the presence of personality disorders.

Interventions

OTHERPeginterferon alfa-2a

Treatment as usual clinical practice

DRUGRibavirin

Treatment as usual clinical practice

Sponsors

Grupo de Enfermedades Infecciosas de la Sociedad Española de Sanidad Penitenciaria
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients 18 years of age. * Patients with expected prison stay beyond the duration of follow-up period of the study. * Patients with chronic HCV infection and detectable viral load to initiate treatment with standard therapy. * Patients their written informed consent to participate in the study.

Exclusion criteria

* Patients previously treated with Interferon (IFN) and Ribavirin (RBV). * Patients can not read or understand a written questionnaire at the discretion of the investigator.

Design outcomes

Primary

MeasureTime frame
Sustained Viral Response (SVR)RNA-VHC at weeks 24 or 48

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 15, 2026