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IT-system Development for Reaching Cervix Cancer Screening Non-attenders

NCT02750124 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8000

Last updated 2020-10-05

No results posted yet for this study

Summary

The main purpose is to develop and test an IT-infrastructure to provide more individualized ways of inviting and reaching women who have not participated, despite having been invited with annual reminders, in cervix cancer screening program during a ten year period.

Conditions

Interventions

DEVICE

Cobas PCR Female swab sample Packet

The cobas® PCR Female Swab Sample Kit is used to collect and transport vaginal swab specimens self-collected.

OTHER

Routine practice

The standard, annual renewed invitation to cervical screening.

Sponsors & Collaborators

Principal Investigators

  • Joakim Dillner, MD · Karolinska Institutet

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
33 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-14
Primary Completion
2016-12-31
Completion
2021-12-31

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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 NCT02750124 on ClinicalTrials.gov