Trial Information
Cervix Cytological Screening - Comparison of Tampon Self-Test and the Routine Smear.
Inclusion Criteria:
1. Women with cervical dysplasia been referred to conisation or
2. Women invited to cervical screening program
Exclusion Criteria:
1. Women not performing the tampon self-test before conisation or
2. Women not performing the tampon self-test af least 1 month after receiving the tampon
Type of Study:
Interventional
Study Design:
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind, Primary Purpose: Screening
Outcome Measure:
Sensitivity and specificity of the tampon self-test
Principal Investigator
Hans Svanholm, consultant
Investigator Role:
Study Director
Investigator Affiliation:
Randers Hospital, Pathological Institute
Authority:
Denmark: Danish Dataprotection Agency
Study ID:
TP06-2351
NCT ID:
NCT00377845
Start Date:
September 2006
Completion Date:
March 2008
Related Keywords:
- Uterine Cervical Dysplasia
- Uterine Cervical Neoplasms
- self test
- PAP smear
- tampon test
- cervical dysplasia
- Neoplasms
- Uterine Cervical Neoplasms
- Uterine Cervical Dysplasia
- Cervical Intraepithelial Neoplasia