Insertion of the Singularity airway device with or without muscle relaxants
Summary description of the study
Laryngeal masks are commonly used airway devices in anesthesia. Singularity is a newly introduced laryngeal mask that has already been studied in our department in 2 studies. Muscle relaxants are also frequently used in anesthesia in connection with airway management, for example during intubation. This study aims to investigate whether the insertion of the Singularity is facilitated by the administration of muscle relaxants. 90 patients will be randomized into 2 groups (insertion with or without muscle relaxant). One inclusion criterion is that the medication is deemed necessary for the operation. The main parameter being investigated is the time required for the insertion of the laryngeal mask.
(BASEC)
Intervention under investigation
Laryngeal mask Singularity (Singularity; Schönenberg, Switzerland)
(BASEC)
Disease under investigation
Patients in general anesthesia with laryngeal mask as airway assistance
(BASEC)
Patient consent, age > 18 years, weight 50 - 100 kg, planned anesthesia with laryngeal mask, muscle relaxants deemed necessary (BASEC)
Exclusion criteria
Pregnancy, emergency surgery, loose teeth, patient refusal (BASEC)
Trial sites
St. Gallen
(BASEC)
Sponsor
Institut für Anästhesie, Spital Thurgau Frauenfeld
(BASEC)
Contact
Contact Person Switzerland
Alexander Dullenkopf
+41581447560
alexander.dullenkopf@clutterstgag.chSpital Thurgau Frauenfeld
(BASEC)
Scientific Information
not available
Name of the authorising ethics committee (for multicentre studies, only the lead committee)
Ethikkommission Ostschweiz EKOS
(BASEC)
Date of authorisation
12.06.2025
(BASEC)
ICTRP Trial ID
not available
Official title (approved by ethics committee)
Prospective evaluation of the Laryngeal Mask Singularity® in adult patients with or without neuromuscular blockade under clinical conditions (BASEC)
Academic title
not available
Public title
not available
Disease under investigation
not available
Intervention under investigation
not available
Type of trial
not available
Trial design
not available
Inclusion/Exclusion criteria
not available
not available
Primary and secondary end points
not available
not available
Registration date
not available
Incorporation of the first participant
not available
Secondary sponsors
not available
Additional contacts
not available
Secondary trial IDs
not available
Results-Individual Participant Data (IPD)
not available
Further information on the trial
not available
Results of the trial
Results summary
not available
Link to the results in the primary register
not available