Informations générales (source: ClinicalTrials.gov)
Establishment of an Artificial Larynx After Total Laryngectomy (LA)
Interventional
N/A
University Hospital, Strasbourg, France (Voir sur ClinicalTrials)
octobre 2011
octobre 2013
29 juin 2024
This study aims to evaluate the effectiveness of an artificial larynx on the restoration
of laryngeal functions, mainly breathing and swallowing.
Etablissements
Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
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Service d'ORL et de Chirurgie Cervico-Faciale, Hôpital de Hautepierre, 1 avenue Molière - 67091 Strasbourg Cedex - Strasbourg - France | Contact (sur clinicalTrials) |
Critères
Tous
Inclusion Criteria:
- Anyone over 18 years, male or female, with a carcinomatous disease of the upper
airways requiring a total laryngectomy
- Anyone over 18 years, male or female, with a carcinomatous disease of the upper
airways requiring a total laryngectomy
- Less than 18 years
- Contraindications to general anesthesia
- Any situation considered by the physician operator as an exclusion
- Pregnant women
- Lactating women
- Subglottic or basi-lingual tumor extension more than 1 cm
- Prior radiotherapy
- Severe coagulation disorders