Informations générales (source: ClinicalTrials.gov)

NCT03738267 Active, sans recrutement
Study on the Occurrence of Head and Neck Cancers During Pregnancy
Observational
  • Tumeurs de la tête et du cou
Centre Francois Baclesse (Voir sur ClinicalTrials)
novembre 2018
mai 2027
29 août 2025
Head and neck cancers that occurred during pregnancy

Etablissements

Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données
CLCC INSTITUT GUSTAVE ROUSSY Ingrid BREUSKIN En recrutement IDF 17/02/2024 12:26:19  Contacter
Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
IFSI AP-HP DE L'HÔPITAL TENON Contact (sur clinicalTrials)
Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Centre François Baclesse - Caen - France Contact (sur clinicalTrials)
Chu Grenoble Alpes - Grenoble - France Contact (sur clinicalTrials)
Chu Poitiers - Poitiers - France Contact (sur clinicalTrials)
Chu Toulouse - Toulouse - France 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
Chu Besancon - Besançon - France Contact (sur clinicalTrials)
Chu Bordeaux - Bordeaux - France Contact (sur clinicalTrials)

Critères

Femme
Inclusion Criteria:

- 18 year old woman or over at the time of participation

- PS 0 -2

- Cancer diagnosed (biopsy date) from 01/01/2010 between the second week of pregnancy
and the 12 months postpartum.

- Primitive may concern the following sites:

oral cavity, nasopharynx, oropharynx, hypopharynx, larynx, prevalent lymphadenopathy,
nasal cavity, salivary glands, dental tumors, ear tumors, paragangliomas optic pathways,
facial sinus / facial mass, nose, ear and other head and neck

- All histologies (epithelial tumors, sarcomas, mucosal melanomas, embryonic tumors,
undifferentiated tumors)

- Patient receiving or having received a specific oncological treatment among surgery,
radiotherapy, chemotherapy, hormone therapy.

- All stages allowed: localized stages and metastatic stages immediately.

- No opposition of the patient to participate in this study



- Any other neoplastic antecedent

- Exclusion of metastases at the level of the VADS of another primitive than a cancer
of the VADS

- Exclusion of hematological tumors (lymphoma) and glial tumors

- Person subject to a legal protection measure or unable to express their consent