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NCT Number: NCT04258449

DOvEEgene Fleur: New Uterine Sampling Tool

This study is related to a previous study from the same group which started in 2014 (NTC02288676, McGill REB A08-M79-13B, MUHC REB 2020-5945) to develop a clinically implementable screening test -DovEEgene: developing and validating a novel molecular test for the early diagnosis of cancer of the endometrium, tubes and ovaries. This study is designed to identify endometrial, tubal and ovarian cancer very early based on identifying cancer-specific mutations (cancer DNA) in a pap sample taken from inside the uterus. The results are particularly encouraging given that control group is challenging with high background mutational burden from benign tumours, endometriosis, germ-line mutations etc.

To date, all the intrauterine samples were obtained using the commercially available TAO brush™ which is designed to take an endometrial sample. However, when patient tolerability was assessed using a numerical pain scale (NPS) ranging from 0 (no pain) to 10 (severe pain), patients rated the sampling using the TAO brush™ at 3.5 versus 0 for a cervical pap sample. These results were not surprising as the TAO brush™ was designed for dislodging strips of endometrial tissue to use for histopathologic examination. With respect to the investigators objective, which is to collect cancer cells that have exfoliated to the uterus, a sampler that collects these exfoliated cells with as little disturbance as possible to the underlying endometrium is preferred. In this sub-study, the investigators aim to evaluate a new endometrial sampling tool, the DOvEEgene Fleur, which is believe to be superior to the current TAO brush™ in terms of cancer detection, ease of use and patient tolerability. The sampler has been designed using materials/components found in the TAO brush™ and other approved medical devices.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Be at least 18 years of age.
  • Have capacity to understand the study.
  • Be able to provide informed consent.
  • If the patient has a recently treated cervical abnormality, she must have had a Pap smear with normal results at least 4 months following treatment by loop electrosurgical excision procedure (LEEP) or cone biopsy.
  • Have suspected or confirmed cancer of the upper genital tract and be undergoing surgery for said tumor removal.

Exclusion criteria

  • Prior hysterectomy.
  • Be pregnant or possibly pregnant.
  • Be nursing, as the device contains phthalates (plasticizers) that "have not been fully characterized and there may be concern for reproductive and developmental effects".
  • Have an infected or inflamed cervix.
  • Have a confirmed or suspected pelvic infection.
  • Have a confirmed or suspected vaginal infection.
  • Have had recent history of uterine perforation.
  • Patients with recently treated cervical abnormalities must have a Pap smear with normal results at least 4 months following treatment by loop electrosurgical excision procedure (LEEP) or cone biopsy in order to be eligible.

Treatment and study plan

DOvEEgene Fleur Sampling

Device

Patients will undergo uterine sampling with DOvEEgene Fleur endometrial sampling device prior to surgical intervention, in addition to standard of care treatment.

Primary outcomes

  1. Patient related outcomes including pain and acceptability

    Time frame: up to 1 year

    Evaluate pain tolerability and acceptability during and after endometrial sample collection. This will be assessed using pain scores reported by participants on numeric pain scale (NPS) ranging from 0 to 10. Final pain scores with the DOvEEgene Fleur will be compared to historical pain scores collected with the TAO brush (Cook Medical).

Secondary outcomes

  1. Feasibility of performing sample collection by clinicians

    Time frame: up to 1 year

    Ease of use of the DOvEEgene Fleur will be evaluated through a physician feedback form.

  2. Quality/quantity of sample collection

    Time frame: up to 1 year

    Molecular assessment to verify DOvEEgene Fleur is capable of detecting cancer cells from the uterus.

Study contacts

Contact information is provided by the study sponsor or research team.

Dr. Claudia Martins, PhD

CONTACT

[email protected]

(514) 934-1934 ext. 35249

Dr. Lucy Gilbert, MD,MSc,FRCOG

CONTACT

[email protected]

(514) 934-1934 ext. 34049

Sponsors and collaborators

Lead sponsor

McGill University

Other

Collaborators

  • GSE Biomedical
  • McGill University Health Centre/Research Institute of the McGill University Health Centre

Registry information

Important dates

Study start
2020
Primary completion
2026
Study completion
2026
First posted
Feb 6, 2020
Registry last updated
Sep 26, 2025

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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