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A Comparison of a Sheathed to a Standard Speculum for Visualization of the Cervix

NCT01670630 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 136

Last updated 2013-03-04

No results posted yet for this study

Summary

The purpose of this study is to estimate if a novel sheathed speculum provides improved visualization of the cervix compared to a standard ("non sheathed") speculum, and to estimate if the sheathed speculum causes less discomfort during the examination.

Conditions

  • Comparison of a Sheathed Versus Standard Plastic Speculum

Interventions

PROCEDURE

Sheathed speculum examination

PROCEDURE

Standard speculum examination

Sponsors & Collaborators

  • MDI Worldwide LLC

    collaborator UNKNOWN

  • AdventHealth

    lead OTHER

Principal Investigators

  • David A Hill, M.D. · AdventHealth

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-07-31
Primary Completion
2013-02-28
Completion
2013-02-28

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 NCT01670630 on ClinicalTrials.gov