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NCT02189954Completed

Effect of Laryngeal Mask Cuff Pressure in Geriatric Patients

Effect of Laryngeal Mask Cuff Pressure on Postoperative Pharyngolaryngeal Complications in Geriatric Patients
Dokuz Eylul UniversityPhase 4ClinicalTrials.govprocedure
Study focus
Disease/Condition
Anaesthesia
Drug/Device/Intervention
The placement according to the manufacturer's instructions
Study type
Interventional
Intervention type
procedure
Sponsor & location
Primary sponsor
Dokuz Eylul University
Location
Izmi̇r, Turkey
Timeline & enrollment
Phase
Phase 4
Start date
Jul 01, 2011
End date
Aug 01, 2012
Enrollment
90 participants
Primary outcome

Postoperative Pharyngolaryngeal Morbidity Postoperative 1.Hour

Summary

Laryngeal Mask is widely used for air-way management during anaesthesia. Pharyngolaryngeal
 morbidity linked to laryngeal mask use is related to correct choice of mask size, placement
 technique, placement of the laryngeal mask in the correct position on the larynx, cuff volume
 and cuff pressure. It has been stated that keeping laryngeal mask cuff pressure below 45 mmHg
 (60 centimeter of water(cmH2O) ) can prevent pharyngolaryngeal morbidity related to laryngeal
 mask (throat pain, dysphonia, dysphagia) and shown that using a manometer after Laryngeal
 Mask Unique placement to limit pressure within the cuff can reduce this morbidity by nearly
 70%. Studies commenting on pharyngolaryngeal morbidity generally do not choose a certain age
 group and cover stages including very young and middle-aged groups. In the literature only
 one similar study on the geriatric age group was found.
 
 The aim of this study is to compare the postoperative pharyngolaryngeal morbidity in a group
 with cuff pressure held to 44 mmHg (60 cmH2O with a manometer and a group with Laryngeal Mask
 cuff inflated without reference to pressure in the geriatric age group with indications for
 Laryngeal Mask Unique placement.

ICD-10 classifications
Anaesthetic, unspecifiedOther and unspecified general anaestheticsOther complications of anaesthesiaLocal anaestheticsAnaesthesia of skin
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT02189954
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT02189954 through Pure Global AI's free database. This Phase 4 trial is sponsored by Dokuz Eylul University and is currently Completed. The study focuses on Anaesthesia. Target enrollment is 90 participants.

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