Royal Victoria Hospital (Glen Site)
Montreal, Quebec, H4A 3J1, Canada
Location status: Recruiting
Location contact
Dr. Claudia Martins, PhD
CONTACT
(514)934-1934 ext. 36794
Dr. Lucy Gilbert, MD,MSc,FRCOG
CONTACT
(514)934-1934 ext. 34049
NCT Number: NCT04258449
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.
Interested in participating?
Request Info18 year and older
Female
Observational
Montreal, Quebec, H4A 3J1, Canada
Location status: Recruiting
Dr. Claudia Martins, PhD
CONTACT
(514)934-1934 ext. 36794
Dr. Lucy Gilbert, MD,MSc,FRCOG
CONTACT
(514)934-1934 ext. 34049
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients will undergo uterine sampling with DOvEEgene Fleur endometrial sampling device prior to surgical intervention, in addition to standard of care treatment.
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).
Time frame: up to 1 year
Ease of use of the DOvEEgene Fleur will be evaluated through a physician feedback form.
Time frame: up to 1 year
Molecular assessment to verify DOvEEgene Fleur is capable of detecting cancer cells from the uterus.
Contact information is provided by the study sponsor or research team.
Dr. Claudia Martins, PhD
CONTACT
(514) 934-1934 ext. 35249
Dr. Lucy Gilbert, MD,MSc,FRCOG
CONTACT
(514) 934-1934 ext. 34049
McGill University
Other
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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