Clinical trial · Observational
Discovery of Microbiome-based Biomarkers for Patients With Cancer Using Metagenomic Approach
Discovery of Microbiome-based Biomarkers for Patients With Cancer Using Metagenomic
NCT04567446CI-TRIAL-00077897ONCOBIOTICSunknownClinicalTrials.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)
Multicentric prospective study with collection of biological samples as part of type II research
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Blood sample | Other | — | UNRESOLVED |
| Stool | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- label
- Patients with bladder cancer who will start cancer treatment
- description
- Collection of biological samples (stool and blood) and data from patients included in the study will be performed: 1. By identifying the patients who will start treatment anticancer (chemotherapy, hormone therapy, immunotherapy). 2. Collection of biological resources (all samples will be collected in fresh): stool and blood 3. Collection of clinical data corresponding to each patient included in the study by a clinical research assistant
- interventionNames
- Other: Stool
- Other: Blood sample
- label
- Patients with Non-Small-Cell Lung cancer who will start cancer treatment
- description
- Collection of biological samples (stool and blood) and data from patients included in the study will be performed: 1. By identifying the patients who will start treatment anticancer (chemotherapy, hormone therapy, immunotherapy). 2. Collection of biological resources (all samples will be collected in fresh): stool and blood 3. Collection of clinical data corresponding to each patient included in the study by a clinical research assistant
- interventionNames
- Other: Stool
- Other: Blood sample
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: * Patient with cancer who will start treatment anticancer (see cohorts). * Patient information and signature of the consent form before any specific procedure for the study. The patient must be able and must be inclined to cooperate in the study procedures. * Patient affiliated to a social security scheme or beneficiary of a similar scheme. Exclusion Criteria: * Pregnant or lactating woman * Patient under guardianship or curatorship or deprived of liberty by a decision judicial or administrative or patient unable to give his consent.
References
Publications (0)
Data not yet available
No reference posted for this study.