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IMproved PRactice Outcomes and Value Excellence in Colposcopy

NCT02185599 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 7555

Last updated 2020-03-13

No results posted yet for this study

Summary

The study will observe and quantify shifts in colposcopy practice and outcome improvements in U.S. community-based cervical screening colposcopy examinations after the introduction of the DySIS colposcope with Advanced Cervical Scan.

The study will collect colposcopy data across multiple sites in two arms; a prospective arm, with DySIS being used for the examination and a retrospective arm, with data retrieved from patient charts.

Conditions

  • High Grade Cervical Intraepithelial Neoplasia

Interventions

DEVICE

DySIS

Colposcopy performed with the DySIS digital colposcope

Sponsors & Collaborators

  • DySIS Medical Inc.

    lead INDUSTRY

Eligibility

Min Age
21 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2017-10-09
Completion
2017-10-09

Countries

  • United States

Study Locations

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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 NCT02185599 on ClinicalTrials.gov