Clinical Trials Directory

Trials / Completed

CompletedNCT01311752

Study of Human Papillomavirus Related Genital Pathology Among HIV Positive Women

Study of Human Papillomavirus Related Genital Pathology Among HIV Positive

Status
Completed
Phase
Study type
Observational
Enrollment
676 (actual)
Sponsor
French National Agency for Research on AIDS and Viral Hepatitis · Other Government
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study is a Multicentre cohort study with inclusion throughout the full duration of the study. The primary objective is the study of human papillomavirus related genital pathology in HIV positive women. The secondary objective are: 1. To study the characteristics of HPV infection and related disease in the context of long term HAART and HIV infection ; 2. To study the characteristics of atypical cells of uncertain significance detected in Pap smears, whose prevalence has dramatically increased in the last years; 3. To describe cervical cancers observed in the cohort 4. To study the evolution of recurrent high-grade lesions after surgery 5. To describe the evolution of vaginal lesions developed after hysterectomy for high-grade lesions ; 6. To describe the specific aspects of surgery for the treatment of cervical lesions according to the specific localization in the endocervix in HIV-positive women ; 7. To study the in situ T cell HPV specific response in cervical lesions and the relationship between virological and clinical parameters, host immune status and natural history of lesions ; 8. To initiate a prospective study on anal HPV infection and related disease among women infected with HIV. 9. To initiate a study on therapeutic and/or prophylactic HPV vaccines in the context of immunosuppression and a high rate of HPV infection ;

Detailed description

Data were be collected into evaluate: * Analysis of prognostic factors (CD4, antiviral therapy) of cervical lesions, using Cox models. * Estimation of rates of Incidence of high grade lesions, of recurrence after surgical treatments using Kaplan Meier tests. * Logistic regression analysis for the study of factors associated with complete excision after surgical treatment. * SIR (standardised incidence rate) evaluation for cervical cancer Study procedures are Annual follow-up in case of normal Pap smear, biannual follow-up in case of cervical lesions. Surgical management of High grade lesions.

Conditions

Interventions

TypeNameDescription
PROCEDUREsurgical management of high grade lesionsClinical, pathological and biological, data at diagnosis and during follow-up will be collected. Surgical sample will be collected to study human papillomavirus related genital pathology.

Timeline

Start date
2007-11-01
Primary completion
2012-11-01
Completion
2012-12-01
First posted
2011-03-09
Last updated
2012-12-27

Source: ClinicalTrials.gov record NCT01311752. Inclusion in this directory is not an endorsement.