Informations générales (source: ClinicalTrials.gov)

NCT04746729 En recrutement IDF
Health Effects of CArdiac FluoRoscopy and MOderN RadIotherapy in PediatriCs - Radiotherapy (HARMONIC-RT)
Observational [Patient Registry]
  • Tumeurs
  • Tumeurs radio-induites
Institut National de la Santé Et de la Recherche Médicale, France (Voir sur ClinicalTrials)
janvier 2021
janvier 2042
05 août 2026
The goal of the HARMONIC-RT study is to evaluate late health and social outcomes of contemporary techniques of external beam radiotherapy in paediatric patients, based on the setting-up of a European, long-term registry complemented by a biobank.
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Etablissements

Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données
CLCC INSTITUT GUSTAVE ROUSSY Noura SELLAMI En recrutement IDF 01/09/2026 18:20:03 Contact (sur clinicalTrials)
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Centre Régional François Baclesse - Caen - France Juliette Thariat, MD En recrutement Contact (sur clinicalTrials)
Gustave Roussy - Villejuif - France Stéphanie Bolle En recrutement Contact (sur clinicalTrials)

Critères

Tous


- First external beam radiation therapy (EBRT) started in 2000 or after for management
of a first primary neoplasm

- Age under 22 years at the time of first EBRT initiation

- Radiation treatment plan (first EBRT) stored in DICOM format

- Usual residency in the country of EBRT to enable a long-term follow-up

Exclusion Criteria:

- Patients with poor prognosis (e.g. diffu


- Patients with poor prognosis (e.g. diffuse pontine glioma or high grade glioma) at
first EBRT initiation

- Prior external or internal radiation therapy

- Patients who refused to participate in the study

Prospective inclusion of study participants

Inclusion Criteria:

- Scheduled first EBRT for management of a first primary neoplasm

- Age under 22 years at the time of scheduled first EBRT

- Radiation treatment plan stored in DICOM format

- Affiliate or beneficiary of health insurance (or any required equivalent as defined
in applicable national law)

- Usual residency in the country of EBRT to enable a long-term follow-up

- Signed informed consent/assent

Exclusion Criteria:

- Patients with poor prognosis (e.g. diffuse pontine glioma or high grade glioma)

- Prior external or internal radiation therapy;

- Protected adults (persons under curatorship, tutorship / individuals under
guardianship by court order, persons deprived of their liberty)

- Adult/parent(s)/legal representative(s) who cannot read or understand the informed
consent in the applicable language(s) in the country of EBRT