Investigation of the Uterine Cervix Using CervicalMD

NCT ID: NCT00839475

Last Updated: 2010-03-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

26 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-06-30

Study Completion Date

2009-07-31

Brief Summary

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The purpose of this study is to demonstrate the CervicalMD device's ability to collect digital imagery suitable for a colposcopy examination.

Detailed Description

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Conditions

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Colposcopy

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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Inclusion Criteria

* Female
* Negative Pregnancy test
* Abnormal Pap smear
* 18 years and older
* Presence of a cervix

Exclusion Criteria

* Pregnant
* Absence of a cervix
* Less than 18 years old
* Male
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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STI-Medical Systems

INDUSTRY

Sponsor Role lead

Responsible Party

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STI-Medical Systems,

Principal Investigators

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Daron G Ferris, MD

Role: PRINCIPAL_INVESTIGATOR

Augusta University

Other Identifiers

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2008-1

Identifier Type: -

Identifier Source: org_study_id

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