Actively Recruiting
Study Evaluating the Efficacy of the myDIET Software Tool in the Nutritional Management of Patients With Localized and Resectable Gastric or Esogastric Junction Cancer.
Led by Centre Leon Berard · Updated on 2026-04-28
60
Participants Needed
1
Research Sites
235 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a prospective, single-center, single-arm Phase II study evaluating the efficacy of the myDIET software tool in the nutritional management of patients with localized and resectable esogastric junction cancer.
CONDITIONS
Official Title
Study Evaluating the Efficacy of the myDIET Software Tool in the Nutritional Management of Patients With Localized and Resectable Gastric or Esogastric Junction Cancer.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient 18 years of age or older at date of signing informed consent to participate
- Histologically proven diagnosis of gastric adenocarcinoma or OGJ
- Localized, resectable disease
- Indication for perioperative chemotherapy and/or immunotherapy validated in multidisciplinary consultation meeting
- Scheduled surgery date at least 1 month after enrolment
- Performance status (ECOG) of 0 to 2
- Membership of a social security scheme
- Signed informed consent to participate
You will not qualify if you...
- Presence of other associated solid cancer or haemopathy
- Severe comorbidity with Charlson index greater than 9
- Presence of unbalanced dysthyroidism
- History of gastric, duodenal, or esophageal surgery
- Inability to comply with study requirements, including inability to connect to myDIET, difficulty understanding written French, psychological or physical incapacity
- Patient under guardianship, curatorship, or safeguard of justice
- Participation in another clinical trial or interventional study likely to interfere with the primary endpoint
- Pregnant or breastfeeding patient
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Centre Léon Berard
Lyon, France, 69008
Actively Recruiting
Research Team
P
Pamela Funk-Debleds, MD
CONTACT
C
Clélia Coutzac, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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