Last reviewed · How we verify

NCT06213051: HPV

Comparison of Self-collection Using Dry Compared to Wet Swabs for HPV Detection

Status unknown Last updated 29 July 2024
What this trial tests

trial testing • COPAN Self-collection FLOQSwabs® (COPAN, Italy) in Human Papillomavirus Infection in 1,306 participants. Status unknown.

Timeline
25 July 2024
Primary endpoint
30 September 2024
30 September 2024

Quick facts

Lead sponsorFoundation for Innovative New Diagnostics, Switzerland
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment1,306
Start date25 July 2024
Primary completion30 September 2024
Estimated completion30 September 2024

Drugs / interventions tested

Conditions studied

Sponsor

Foundation for Innovative New Diagnostics, Switzerland

Who can join

Adults 30 to 80, female only, with Human Papillomavirus Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will compare the performance of self-collected vaginal swabs, transported without liquid media (dry swabs) and self-collected vaginal swabs, transported in liquid media (wet swabs) for detection of hrHPV DNA LBC as the reference standard.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Human Papillomavirus Infection

Currently open trials in the same condition.

Other Foundation for Innovative New Diagnostics, Switzerland trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06213051.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing