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Be Part of Research - Trial Details - Can the iKnife Distinguish Between Normal and Malignant Endometrial Tissue?

Can the iKnife Distinguish Between Normal and Malignant Endometrial Tissue?

Completed

Open to: FEMALE

Age: 18.0 - N/A

Medical Conditions

Endometrial Neoplasms
Endometrial Cancer
Endometrial Hyperplasia
Endometrial Diseases


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Aim: Determine if Rapid Evaporative Ionization Mass Spectrometry (the iKnife); can diagnose cancer and pre-cancer from endometrial tissue biopsy samples.

Women attending a gynaecology clinic for assessment of abnormal bleeding will receive an pelvic (internal) ultrasound as routine standard of care. If any abnormalities are detected, a tissue sample will be needed. If women are agreeable a second tissue sample will be taken for research. The first will be analysed by conventional means (histopathology). The second sample with new technology called the 'iKnife'. This is a modified type of Mass spectrometry device, that separates particles based on their mass charge ratio. The idea being that if tissue is burnt, gas is produced, and this gas contains lots of ions that can be analysed by the iKnife. Each type of tissue (cancer or non-cancer) will have a unique signature that the iKnife can use to distinguish between samples. If effective it could be used in future outpatient clinics to provide a one-stop, true point of care diagnosis.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Jun 2017 Jun 2019

INTERVENTIONAL

Intervention Type : DIAGNOSTIC_TEST
Intervention Description : The endometrial tissue will be analysed by this new technology and compared to gold standard (histopathology)

Intervention Arm Group : All patients;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Queen Charlotte and Hammersmith Hospital
    London
    W12 0HS


The study is sponsored by Imperial College London




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Read full details for Trial ID: NCT03207074
Last updated 26 June 2020

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