Overview
The Effects of Beclomethasone Upper the Endotracheal Cuff on the Occurrence of Sore Throat at Extubation
Status:
Withdrawn
Withdrawn
Trial end date:
2017-09-01
2017-09-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The aim of the study is to test the effectiveness of a solutions of beclomethasone repeatedly instilled through the supraglottic line of the endotracheal tube on post-extubation airway disturbances related to tracheal intubation. The primary endpoint will be the decrease of the incidence of sore-throat 15 minutes and 12 hours after extubation. Secondary endpoints will regard the effects on hoarseness and cough.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Policlinico Universitario Agostino GemelliTreatments:
Beclomethasone
Criteria
Inclusion Criteria:- intensive care postoperative admission
- tracheal intubation for a total lapse of time between 10 and 18 hours
Exclusion Criteria:
- age < 18,
- hypersensitivity to FANS and/or corticosteroids,
- a medical history positive for diseases affecting upper airways or trachea or causing
cough, hoarseness, or voice disorders;
- intubation after more than two attempts or with aids (i.e. stylets, Airtraq,
Glidescope, Fibroscopy).