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NCT05679141

Clinical Correlation Between Self-collected and Physician-collected HPV Screening Kits

Completed Last updated 26 April 2024
What this trial tests

trial in HPV Infection in 344 participants. Completed in 19 March 2024.

Timeline
1 February 2023
Primary endpoint
19 March 2024
19 March 2024

Quick facts

Lead sponsorSwitch Health Solutions Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment344
Start date1 February 2023
Primary completion19 March 2024
Estimated completion19 March 2024
Sites1 location across Canada

Conditions studied

Sponsor

Switch Health Solutions Inc.

Who can join

21 and older, female only, with HPV Infection or Cervical Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study is to validate the of the Evalyn®Brush via self-collection to the standard clinician-collected technique using the BD SurePath™ collection vial and Rovers CombiBrush for detection of Human Papillomavirus (HPV). This study will validate the sensitivity and specificity of the Evalyn Brush with the future goal of making this testing approach available for self-collection in the future.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for HPV Infection

Currently open trials in the same condition.

Other Switch Health Solutions Inc. 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/NCT05679141.

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