NCT03750214

Evaluation of the Biop Colposcopy System's Safety and Performance (Accuracy of Its Registration Procedure)

Bio Colposcopy System CIP: Evaluation of the Biop Colposcopy System's Safety and Performance (Accuracy of Its Registration Procedure)

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 26 (estimated)
• Sponsor: BIOP Medical · Industry
• Sex: Female
• Age: 22 Years – 65 Years
• Healthy volunteers: Not accepted

Summary

This is a multi-center, prospective, non-randomized, confirmatory study to evaluate the safety and performance of the Biop Digital Colposcope and the accuracy of the image registration procedure between the Biop Digital Colposcope unit and the Biop Micro Colposcope probe unit.

Detailed description

This is a multi-center, prospective, non-randomized, confirmatory study to evaluate the safety and performance of the Biop Digital Colposcope and the accuracy of the image registration procedure between the Biop Digital Colposcope unit and the Biop Micro Colposcope probe unit. The Biop Digital Colposcope is intended for magnified viewing of the tissues of the vagina, cervix and external genitalia in order to assist doctors in diagnosing abnormalities such as lesions or cancer, and selecting areas for biopsy. The images from the digital colposcope are to be viewed on a color display. The digital colposcope is intended for use in hospitals, clinics, and doctor's offices. The Biop Micro Colposcope probe unit is an imaging tool intended to be placed in the vagina for acquisition of images of the cervix. It is intended as an adjunct to the Biop Digital Colposcope. It should NOT be used as a substitute for a thorough colposcopic evaluation. The Biop Micro Colposcope Probe unit is not intended for use on the vulva and vagina. It is anticipated that it will take approximately 3 months to complete active enrollment. Study duration for each subject is 1-2 days, including screening, enrolment and procedure. The study will be completed when the final study subject has completed the procedure. 1. Performance - to confirm that average image registration error is less than or equal to (≤) 2mm. 2. Safety - to evaluate the safety of the Biop Digital Colposcope in women undergoing cervical colposcopy procedures.

Conditions

• Cervical Cancer Screening

Interventions

Type	Name	Description
DEVICE	Biop Colposcopy System	The procedure stages: 1. Scanning of the cervix - the cervix is scanned using the micro colposcope probe unit, to produce a total of 51 micro-images and one macro image from the panoramic camera. 2. Colposcopy exam - during the standard colposcopy exam, the doctor acquires a panoramic image of the cervix with the digital colposcope. 3. A questionnaire completed by the subject after the Biop procedure, with regards to any unusual sensations or events experienced during the procedure. 4. A questionnaire completed by the user after the Biop procedure, with regards to system usage 5. Image Registration analysis

Timeline

• Start date: 2020-05-01
• Primary completion: 2020-11-01
• Completion: 2020-12-01
• First posted: 2018-11-21
• Last updated: 2020-01-18