Actively Recruiting
B-GLUCANCER2 : A Pilot Study Evaluating a New Method for Cancer Detection by Measuring the Activity of Different Glycosidase Enzymes in the Plasma of Patients With a Localized Cancer.
Led by Poitiers University Hospital · Updated on 2026-02-05
220
Participants Needed
1
Research Sites
108 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to develop a new cancer diagnostic and prognostic tool based on the dynamic and non-invasive detection of an exogenous volatile molecule, i.e., ethanol, from patients' samples. Patients' blood plasma will be analyzed with a mixture of volatile organic compound-based probes, each targeting a specific glycosidase. The presence of a given glycosidase in a blood sample would thus be revealed by the detection of an ethanol isotope in the gas phase. 3 groups of patients with localized cancer (breast, prostate, pancreas) will be enrolled, as well as 1 group of patient without any cancer (control group). For the patients, two 5ml plasma samples will be collected, one before and one after surgery for localized cancers. For healthy volunteers, only one 5ml plasma sample will be collected. The primary objective will be to compare the levels of glycosidases measured in the blood of patients followed for localized cancer and referred for first surgery compared to control patients without cancer.
CONDITIONS
Official Title
B-GLUCANCER2 : A Pilot Study Evaluating a New Method for Cancer Detection by Measuring the Activity of Different Glycosidase Enzymes in the Plasma of Patients With a Localized Cancer.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older
- Group 1: Patients with confirmed, untreated, localized breast cancer scheduled for initial surgery
- Group 2: Patients with confirmed, untreated, localized lung cancer scheduled for initial surgery
- Group 3: Patients with confirmed, untreated, localized pancreatic cancer scheduled for initial surgery
- Group 4: Control patients with no diagnosis or history of solid or blood-related cancer
You will not qualify if you...
- Refusal to participate in the study
- Minors, pregnant or breastfeeding women
- Individuals deprived of liberty by judicial or administrative decision
- Persons residing in social care facilities
- Adults under legal protection
- Cancer patients undergoing oncological treatment
- Cancer not confirmed by tissue examination
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
C.H.U. Poitiers
Poitiers, France, 86000
Actively Recruiting
Research Team
S
Sheik Emambux, MD PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
4
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