Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:59 PM
Ignite Modification Date:
2025-12-24 @ 4:59 PM
NCT ID:
NCT05848050
Eligibility Criteria:
Inclusion Criteria:
* Patient aged 18 or over;
* Patient with cerebral metastases from a solid cancer, at least one of which is accessible to surgical excision (contrast enhancement of at least 1 cm);
* Patient able to understand the information related to the study and to read the information leaflet;
* Patient having signed a written informed consent to participate in the study.
Exclusion Criteria:
* Patient with a medical contraindication to surgery and anesthesia;
* Patient whose anatomical location of the cerebral metastasis contraindicates wide resection;
* Patient with a contraindication to performing a lumbar puncture;
* Pregnant, parturient or breastfeeding women;
* Patient participating in another clinical trial, or in a period of exclusion from another clinical trial;
* Patient under guardianship or curatorship, or under a regime of deprivation of liberty;
* Patient not benefiting from a social security scheme.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT05848050
Study Brief:
Protocol Section:
NCT05848050