Clinical trial · Interventional
Study Evaluating the Efficacy of the myDIET Software Tool in the Nutritional Management of Patients With Localized and Resectable Gastric or Esogastric Junction Cancer.
Evaluation of the Efficacy of the myDIET Software Tool in the Nutritional Management of Patients With Localized and Resectable Gastric or Esogastric Junction Cancer.
NCT06385691CI-TRIAL-00109692MyDIETrecruitingPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Gastric Cancer | Malignant Gastric Neoplasm | CURATED_BROADER | 0.80 |
| Oesogastric Junction Cancer | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| myDIET software tool | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- use of myDIET tool for nutritional management
- description
- Patients will be followed up at regular intervals during neoadjuvant treatment, perioperatively and up to 6 months after the date of surgery (after completion of postoperative treatment).
- interventionNames
- Other: myDIET software tool
Primary outcomes (1)
- measure
- Proportion of patients starting adjuvant treatment within 2 months
- timeFrame
- 2 months after surgery
- description
- proportion of patients for whom adjuvant treatment could be initiated within 2 months after surgery
Secondary outcomes (27)
- measure
- Adherence to the tool
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * 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; * Patients with an indication for perioperative chemotherapy and/or immunotherapy validated in multidisciplinary consultation meeting, with a scheduled surgery date at least 1 month after enrolment; * Performance status (ECOG): 0-2; * Membership of a social security scheme; * Signed informed consent to participate. Exclusion Criteria: * Other associated solid cancer or haemopathy; * Presence of severe comorbidity (Charlson index \> 9) * Presence of unbalanced dysthyroidism; * History of gastric, duodenal or esophageal surgery; * Inability to comply with study requirements, including : * Impossibility for the patient or his/her caregiver to connect to myDIET; * Difficulty in understanding the written French language; * Psychological incapacity (e.g. excessive vulnerability, psychiatric disorder) or physical incapacity (e.g. physical/motor disability); * Patient under guardianship, curatorship or safeguard of justice; * Patients already participating in a clinical trial or interventional study likely to interfere with the evaluation of the primary endpoint. * Pregnant or breast-feeding patient.
References
Publications (0)
Data not yet available
No reference posted for this study.