Official Title
DOvEEgene Fleur: New Uterine Sampling Tool
Brief Title
DOvEEgene Fleur: New Uterine Sampling Tool
Protocol ID
NCT04258449
Lead Sponsor
McGill University
Brief Summary
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.
Study Period
-
Enrollment Count
40 participants
Eligibility Criteria
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.
Filters
Women With Suspected or Confirmed Gynecological Disease
RECRUITING
ADULT
OLDER_ADULT