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Self-Sampling in Women Who Do Not Undergo Routine Cervical Screening

NCT00977392 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3000

Last updated 2013-08-07

No results posted yet for this study

Summary

RATIONALE: Women who do not undergo routine cervical screening may be more likely to collect a self-sample for human papillomavirus testing.

PURPOSE: This randomized clinical trial is studying self-sampling in women who do not undergo routine cervical screening.

Conditions

  • Health Status Unknown
  • Precancerous Condition

Interventions

BEHAVIORAL

compliance monitoring

OTHER

cervical Papanicolaou test

OTHER

educational intervention

OTHER

screening questionnaire administration

OTHER

survey administration

PROCEDURE

colposcopy

Sponsors & Collaborators

  • Barts and the London School of Medicine and Dentistry

    lead OTHER

Principal Investigators

  • Anne Szarewski, MD · Queen Mary University of London

Eligibility

Min Age
25 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2010-02-28
Completion
2011-03-31

Countries

  • United Kingdom

Study Locations

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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 NCT00977392 on ClinicalTrials.gov