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Patient Compliance to Self-collection for Detection of HPV-DNA

NCT02431520 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2015-05-06

No results posted yet for this study

Summary

A study to investigate the compliance of unassisted women to self-collection of specimens for Hybrid Capture (HC) for detection of Human Papilloma Virus (HPV) DNA compared to Pap smear collection by medical personnel, as screening method to identify precursor lesions of cervical cancer.

Conditions

Interventions

PROCEDURE

Self-collection

Women allocated to this arm will be asked to obtain a specimen of vaginal/cervical by self-collection for HCII.

PROCEDURE

Gynecologist collection

Women allocated to this arm will be asked to attend to medical office to have their Pap smear obtained by a gynecologist

Sponsors & Collaborators

  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.

    collaborator OTHER_GOV

  • Oswaldo Cruz Foundation

    lead OTHER

Principal Investigators

  • Fabio B Russomano, MD, PhD · IFF/Fiocruz

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
59 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-05-31
Primary Completion
2007-09-30
Completion
2007-12-31

Countries

  • Brazil

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02431520 on ClinicalTrials.gov