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Colorectal Cancer Detection by Means of Optical Fluoroscopy

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Fondazione IRCCS Istituto Nazionale dei Tumori, Milano

Status

Unknown

Conditions

Colorectal Cancer

Treatments

Device: Optical Fluoroscopy

Study type

Interventional

Funder types

Other

Identifiers

NCT01286064
INT-D178768

Details and patient eligibility

About

The aim of the present prospective study was to investigate the fluorescence emission of human blood plasma of patients with colorectal cancer.

For years, serum tumor markers have been studied for the diagnosis and follow-up of colorectal cancer, among which carcinoembryonic antigen (CEA) has achieved promising results. However, the sensitivity of CEA for colorectal cancer is less than 25% and elevated CEA levels also occur in patients with benign disease, as well as in patients with other carcinomas. Nevertheless, surveillance programs are often based on the CEA test and combination with other markers is at present a matter of research. Alternative methods based on optical fluoroscopy have been introduced in experimental stages for clinical diagnosis of cancer. Few studies have been reported on the application of native fluorescence spectroscopy of biofluids in the diagnosis of tumoral diseases. The above reported findings prompted us to investigate the fluorescence emission of human blood plasma of patients with colorectal cancer. For this purpose, the blood of patients was collected and the fluorescence Preliminary measurements on plasma of patients bearing colon cancer showed that the fluorescence spectra were mainly characterized by the presence of an emission peaking at 620-630 nm, whose excitation spectrum peaked at 405 nm. Hence, an excitation wavelength of 405 nm was selected for the study. The fluorescence emission spectra were recorded in the range of 430-700 nm.

Full description

Eligibility criteria: Gastrointestinal disease or clinical symptoms related to colorectal cancer risk submitted to endoscopy. Exclusion criteria consisted of age younger than 18 years, history of psychiatric illness, and preoperative radiotherapy.

Outcome: investigated the possible role of the native fluorescence of blood plasma in the management of colorectal cancer (CRC) and its feasibility as a new tumor marker. Sample of blood was collected from asymptomatic blood donors and from CRC patients. The native fluorescence of blood plasma was measured using a conventional spectrofluorimeter.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Gastrointestinal disease clinical symptoms related to colorectal cancer risk endoscopy

Exclusion criteria

Age younger than 18 years or more than 75 years, history of psychiatric illness, preoperative chemo/radiotherapy.

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

200 participants in 2 patient groups

patient with colo-rectal cancer
Experimental group
Description:
fluorescence spectra will be mainly characterized by the presence of an emission peaking at 620-630 nm
Treatment:
Device: Optical Fluoroscopy
Device: Optical Fluoroscopy
patient without colo-rectal cancer
Active Comparator group
Description:
fluorescence spectra will be characterized by the absence of an emission peaking at 620-630 nm
Treatment:
Device: Optical Fluoroscopy
Device: Optical Fluoroscopy

Trial contacts and locations

1

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Central trial contact

vannelli alberto, MD

Data sourced from clinicaltrials.gov

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