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Cervix Cytological Screening - Comparison of Tampon Self-Test and the Routine Smear.

NCT00377845 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2008-03-27

No results posted yet for this study

Summary

The purpose of this study is to compare suitability, specificity and sensitivity of the routine smear and the tampon self-test women perform at home.

Study hypothesis: The tampon self-test correspond to the routine cervical smear.

Conditions

  • Uterine Cervical Dysplasia
  • Uterine Cervical Neoplasms

Interventions

PROCEDURE

Regular Tampax used in 3 hours

Sponsors & Collaborators

  • University of Aarhus

    lead OTHER

Principal Investigators

  • Hans Svanholm, consultant · Randers Hospital, Pathological Institute

Study Design

Allocation
NON_RANDOMIZED
Purpose
SCREENING
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
23 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2006-09-30
Primary Completion
2007-12-31
Completion
2008-03-31

Countries

  • Denmark

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 NCT00377845 on ClinicalTrials.gov