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Search / Trial NCT05977803

Contribution of the CEST Sequence in the Characterization of Radionecrosis of Brain Metastases of Pulmonary Origin

Launched by ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS · Aug 3, 2023

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Radionecrosis, Metastases,

ClinConnect Summary

This clinical trial is studying a new imaging technique called the CEST sequence to see if it can effectively diagnose radionecrosis, a condition where brain tissue is damaged after radiation therapy for lung cancer. Researchers want to find out if this new method is just as good as the standard imaging technique currently used, which involves a special type of MRI with contrast dye. The goal is to improve how doctors identify and understand changes in brain metastases, which are cancerous growths that have spread to the brain from lung cancer.

To participate in this study, individuals must be over 18 years old, have a confirmed diagnosis of lung cancer, and have received radiation treatment for their brain metastases. They should also have experienced changes in their brain lesions as seen on follow-up MRI scans. Participants will undergo imaging tests to help researchers compare the new method with the standard approach. It’s important to know that individuals who cannot undergo MRI scans or who have severe cognitive impairments that prevent them from giving consent will not be eligible to participate.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients \> 18 years of age
  • Histologically proven primary lung cancer
  • Histologically proven or not brain metastases
  • Irradiated metastases
  • Inclusion in a treatment protocol for brain metastases by brain metastasis in toto or stereotactic or gamma-knife radiotherapy
  • Morphological increase of one or more lesions of secondary brain metastases on a follow-up MRI
  • Patients affiliated to a social security scheme
  • Exclusion Criteria:
  • Opposition to the study
  • Contraindication to MRI
  • Refusal of imaging by the patient
  • Patient with state medical aid (unless exemption from affiliation)
  • Severe cognitive impairment making informed consent impossible
  • Patients under guardianship or deprived of liberty

About Assistance Publique Hôpitaux De Paris

Assistance Publique - Hôpitaux de Paris (AP-HP) is a leading public hospital system in France, renowned for its commitment to healthcare excellence and innovative medical research. As a prominent clinical trial sponsor, AP-HP plays a pivotal role in advancing medical knowledge and improving patient care through rigorous scientific investigations across a wide range of therapeutic areas. With a focus on collaboration and interdisciplinary approaches, AP-HP leverages its extensive network of hospitals and expert clinicians to facilitate high-quality clinical trials that adhere to the highest ethical and regulatory standards, ultimately aiming to translate research findings into tangible health benefits for diverse patient populations.

Locations

Paris, , France

Patients applied

0 patients applied

Trial Officials

Augustin Gaudemer, MD

Principal Investigator

Assistance Publique - Hôpitaux de Paris

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported