Validation of Transvaginal Tactile Imaging

NCT01491334 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 158

Last updated 2014-02-25

No results posted yet for this study

Summary

The purpose of this study is to validate safety and effectiveness in assessment of the female pelvic floor tissue, and, assess the ability of Vaginal Tactile Imager (VTI) to detect early prolapse conditions and characterize the outcome of reconstructive surgery.

Conditions

  • Pelvic Organ Prolapse

Sponsors & Collaborators

  • National Institute on Aging (NIA)

    collaborator NIH
  • Artann Laboratories

    lead INDUSTRY

Principal Investigators

  • Vladimir Egorov, Ph.D. · Artann Laboratories, Inc.

Eligibility

Min Age
21 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2013-09-30
Completion
2013-11-30

Countries

  • United States

Study Locations

More Related Trials

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 NCT01491334 on ClinicalTrials.gov