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NCT02446379: CLIO

Use of the EnLightTM and LightPathTM Imaging Systems in Gastrointestinal Tumour Surgery

Withdrawn Last updated 26 January 2017
What this trial tests

trial testing The marketed product 2-5 MBq/kg 18F-fluorodeoxyglucose in Gastric Cancer. Withdrawn.

Quick facts

Lead sponsorLightpoint Medical Limited
StatusWithdrawn
Study typeOBSERVATIONAL
Primary completion1 January 2016
Sites1 location across Hungary

Drugs / interventions tested

Conditions studied

Sponsor

Lightpoint Medical Limited — full company profile →

Who can join

30 and older, any sex, with Gastric Cancer or Pancreatic Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will evaluate the performance of the EnLightTM and LightPathTM Imaging Systems in detecting tumour lesions in patients with gastric, pancreas, bile duct or duodenal cancer. EnLightTM will be used to detect positron emission and the LightPathTM system to detect Cerenkov Luminescence. Both are emitted by the Positron Emission Tomography (PET) agent. The study will also evaluate the patient safety and radiation safety of the EnLightTM, and the safety for the device operators and surgical staff of the LightPathTM Imaging System.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Cerenkov luminescence imaging (CLI) for image-guided cancer surgery.
    Grootendorst MR, Cariati M, Kothari A, Tuch DS, et al · · 2016 · cited 54× · PMID 27738626 · DOI 10.1007/s40336-016-0183-x

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