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Completed

NCT Number: NCT04099121

Evaluation of 3D Translabial Ultrasound Imaging for Pessary Size Estimation

Symptoms of female pelvic floor dysfunction, such as incontinence and pelvic organ prolapse, can be alleviated by using pessaries, which are passive medical devices that are inserted in the vagina to support the pelvic organs. Currently, pessaries are fit through trial and error after manual examination, the accuracy of which depends on the physician's expertise level.

The objective of this study is to evaluate the feasibility of using 3D translabial ultrasound imaging of the vagina at various distension volumes to predict the pessary size for successful fit. Ultrasound images will be obtained using commercially available 3D ultrasound probes (Philips, Netherlands), as well as a commercially available 2D ultrasound probe (Philips, Netherlands), which is linearly scanned to capture a 3D volume. The linear scanning will be performed by attaching the 2D probe to a motorized hand-held scanner, which is used to tilt and move the probe to acquire images. Please note that the hand-held scanner does not come in contact with the patient. To distend the vagina, a sterile bag is inserted in the vagina and gradually filled with water using a commercially available urodynamic system (Laborie, Canada) until the vaginal capacity is reached, without causing any discomfort to the patient. This image acquisition technique, previously reported in the literature, is referred to as 3D ultrasound vaginal manometry in this study.

To achieve the objective of this project, 35 pelvic organ prolapse patients, who (i) are current pessary users, (ii) can perform self-care of the pessary, and (iii) can provide informed consent, will be invited to participate in the study. Patients will be asked to remove their pessary prior to ultrasound imaging. Then, 3D ultrasound vaginal manometry will be performed, using the technique described above. Ultrasound images will be analyzed once data acquisition is completed. The size of the pessary estimated from ultrasound images will be compared with the actual pessary size used by the patient.

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Key information

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Victoria Hospital

London, Ontario, N6A 5W9, Canada

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Current pessary users (> 6 months) who have no pessary related complication, including discomfort, repeated vaginal bleeding, and pessary extrusion
  • Are able to provide informed consent
  • Can perform self-care, i.e. removing and inserting the pessary themselves
  • Are willing to remove their pessary 2 days before the ultrasound examination date.

Exclusion criteria

  • Inability to give informed consent
  • Inability to communicate with the person performing the consent and the sonographer performing ultrasound scanning
  • History of pelvic radiation or surgery, (including hysterectomy)
  • Using pessaries other than ring, incontinence dish, donut, Shaatz, Marland, or Gellhorn.
  • Inability to perform the Valsalva maneuver or pelvic floor contraction
  • Restricted mobility that prevents them from ambulating to assess the comfort level of the pessary during the initial pessary fitting visit.
  • Lack of sensation at the pelvic floor.
  • Being pregnant at the time of the examination.

Treatment and study plan

Ultrasound Imaging

Device

3D ultrasound of the pelvic floor and vaginal cavity will be obtained by using a commercial ultrasound system.

Primary outcomes

  1. FEASIBILITY: The predicted pessary size

    Time frame: Up to 3 months following data collection

    The predicted pessary size in cubic mm will be compared with the actual size of the pessary used by the patient

  2. FEASIBILITY: The predicted pessary shape

    Time frame: Up to 3 months following data collection

    The predicted pessary shape will be compared with the actual shape of the pessary used by the patient by calculating the DICE coefficient.

Sponsors and collaborators

Lead sponsor

Western University, Canada

Other

Collaborators

  • Cosm Medical

Registry information

Official study title

Evaluation of 3D Ultrasound Vaginal Manometry for Estimating the Optimal Pessary Size for Patients With Pelvic Organ Prolapse

Important dates

Study start
2020
Primary completion
2023
Study completion
2023
First posted
Sep 23, 2019
Registry last updated
Apr 30, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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