Actively Recruiting
Evaluation of a New Method for Detecting Cancer by Measuring Glycosidase Activity in Plasma of Patients With Localized Cancer - Pilot Study B-GLUCANCER2
Led by Poitiers University Hospital · Updated on 2026-02-05
220
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating a new method to detect and assess cancer by measuring the activity of specific enzymes called glycosidases in patients' blood plasma. This pilot study involves patients with localized breast, lung, or pancreatic cancer, as well as a group of people without cancer, to compare enzyme levels and evaluate the diagnostic potential of this approach. The study is sponsored by Poitiers University Hospital and focuses on early-phase research. Participants with localized cancers will provide two 5ml blood plasma samples, one before surgery and another one month after surgery, to analyze enzyme activity. Healthy volunteers will provide a single 5ml blood plasma sample. The study groups include patients with breast, lung, and pancreatic cancer, alongside a control group with no history of cancer. During the study, researchers will monitor enzyme levels using volatile organic compound-based probes that detect specific glycosidases by identifying ethanol isotopes in the gas phase of blood samples. The primary outcome is to compare enzyme activity before and after surgery in cancer patients versus controls. Secondary outcomes include comparisons among cancer types and over time. Participation involves blood draws and follow-up visits, lasting until one month after surgery for cancer patients or a single visit for healthy volunteers.
CONDITIONS
Brief 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
- Patients with definitively diagnosed, untreated, localized solid breast cancer referred for initial surgery
- Patients with definitively diagnosed, untreated, localized solid lung cancer referred for initial surgery
- Patients with definitively diagnosed, untreated, localized solid pancreatic cancer referred for initial surgery
- Control patients with no diagnosis or history of solid or blood-related cancer
You will not qualify if you...
- Refusal to participate in the research
- Minors
- Pregnant or breastfeeding women
- Persons deprived of liberty by judicial or administrative decision
- Persons staying in social care facilities
- Adults under legal protection
- Cancer patients currently receiving oncological treatment
- Cancer not confirmed by anatomopathological examination
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to the day of surgery
Participants provide blood samples before surgery to measure glycosidase enzyme activity for cancer detection.
1 visit (in-person) before surgery
Duration - 1 day or as needed for surgery
Participants with localized breast, lung, or pancreatic cancer undergo initial surgery.
Duration - Approximately 1 month after surgery
Participants provide a follow-up blood sample approximately one month after surgery to compare enzyme levels.
1 visit (in-person) about one month after surgery
Duration - Up to 1 month
Control participants without cancer provide blood samples for comparison purposes.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
C.H.U. Poitiers
Poitiers, France, 86000
Actively Recruiting
Research Team
S
Sheik Emambux, MD PhD
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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