Validation of Transvaginal Tactile Imaging

Artann Laboratories158 enrolled

Overview

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.

1. The device will detect significant differences in tissue elasticity and anatomy for women with normal pelvic floor versus women with prolapse stage 1. 2. The device will detect significant differences in tissue elasticity and anatomy for patients before and after reconstructive surgery. 3. The device will detect significant differences in tissue elasticity and anatomy among 3 groups of patients with prolapse stages 1, 2 and 3. 4. The device will detect significant differences in tissue elasticity among 3 control groups with normal pelvic floor conditions (nulliparous women at age 21-30, parous women at age 31-40, and postmenopausal women).

Study Type

OBSERVATIONAL

Enrollment

158

Conditions

Pelvic Organ Prolapse

Eligibility

Sex: FEMALEMin age: 21 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Subject is female of 21 years or older AND HAS AT LEAST ONE OF THE FOLLOWING * No evidence of pelvic organ prolapse and no prior pelvic surgery * Stage 1 or greater pelvic organ prolapse affecting one or more vaginal compartments and no prior pelvic surgery * Stage 2 or greater pelvic organ prolapse affecting one or more vaginal compartments and reconstructive surgery is scheduled Exclusion Criteria: * Active skin infection or ulceration within the vagina * Presence of a vaginal septum; * Active cancer of the colon, rectum wall, cervix, vaginal, uterus or bladder; * Ongoing radiation therapy for pelvic cancer; * Impacted stool * Recent (less than three months) pelvic surgery; * Significant pre-existing pelvic pain including levator ani syndrome, severe vaginismus or vulvodynia; * Severe hemorrhoids * Surgically absent rectum or bladder * Significant circulatory or cardiac conditions that could cause excessive risk from the examination as determined by attending physician

Locations (2)

Princeton Urogynecology

Princeton, New Jersey, United States

Institute of Female Pelvic Medicine and Reconstructive Surgery

Allentown, Pennsylvania, United States

Outcomes

Primary Outcomes

Effectiveness in assessment of the pelvic floor tissue conditions.

Time frame: Two years.

Ability in early detection of prolapse conditions.

Time frame: One Year

Ability in characterization of the outcome of pelvic floor reconstructive surgery.

Time frame: Two years.

Data from ClinicalTrials.gov

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