Impact on Postoperative Pain of Three Single-use Adult Supraglottic Airway Devices in Short Gener… (NCT03614598) | Clinical Trial Compass
CompletedNot Applicable
Impact on Postoperative Pain of Three Single-use Adult Supraglottic Airway Devices in Short General Anesthetic Under Controlled Ventilation
France546 participantsStarted 2009-04-22
Plain-language summary
The investigators hypothesize that incidence of pharyngolaryngeal postoperative pain caused by the I-gel and LMA-Suprême devices will be ≤ 5%
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* The patient must have given their free and informed consent and signed the consent form
* The patient must be a member or beneficiary of a health insurance plan
* Adult patients \> 18
* ASA score I-III
* Patient scheduled to undergo elective surgery lasting less than two hours under general anaesthetic without tracheal intubation
* The subject is participating in an interventional study, or is in a period of exclusion determined by a previous study
* The subject refuses to sign the consent
* It is impossible to give the subject informed information
* The patient is under safeguard of justice or state guardianship
* The patient is pregnant or breastfeeding
* Emergency surgery
* Sore thoat ≤ 1 month
* Risk of aspiration of gastric contents
* Body mass index (BMI) \> 35
* Patients with expected airway difficulties
* Contra-indication for any of the devices (symptomatic hiatal hernias, pathological obesity, poly trauma or serious injury, delayed gastric emptying, use of opiates during fasting)
* Patients who are not fasting for routine and emergency anesthesia
* Trismus, limited mouth opening, abscess or pharyngoperilaryngeal mass
What they're measuring
1
Incidence of pharyngolaryngeal postoperative pain of the three devices