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Clinical Trials/ISRCTN45527158
ISRCTN45527158CompletedNot Applicable

PRotection by Offering Human papillomavirus Testing on sElf-sampled Cervicovaginal specimens Trial

VU University Medical Center (The Netherlands)0 sites45,000 target enrollmentStarted: December 28, 2006Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
45,000

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Sex
Female

Inclusion Criteria

  • 1. Women invited for the cervical cancer screening program (ages 30 to 60 years), but who are not responding to their invitation as well as their recall (three months after)
  • 2. Residing in the region covered by district health authorities of North Holland and Flevoland (in the Netherlands)

Exclusion Criteria

  • 1. Not called for screening, i.e., ages under 30 years, or over 60 years
  • 2. Actively responded to the invitation or first recall of the cervical screening program by undergoing a cervical smear at the general practitioner
  • 3. Living outside the region covered by district health authorities of North Holland and Flevoland
  • 4. Under follow-up by gynaecologist for previous non-normal cytology, i.e., abnormal cytology and/or CIN three lesion or worse less than two years before inclusion
  • 5. Current pregnancy
  • 6. Status after extirpation of the uterus or amputation of the portio

Investigators

Sponsor
VU University Medical Center (The Netherlands)

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