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Comparison of placement techniques of proseal laryngeal mask.

Comparison of proseal laryngeal mask placement with the new knotted grip technique using gum elastic bougie versus three other standard techniques (digital technique and using introducer tool).

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20598
Enrollment
308
Registered
2013-03-13
Start date
2012-07-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

patients undergoing general anesthesia for elective surgeries with the use of a supraglottic airway device

Interventions

In Group KG, PLM placement was aided by the GEB in a knotted grip while the other three groups (D,IT,L) served as the control group for the PLM placement. In Group D, PLM was placed using digital te

Sponsors

Ministry of Health, Oman http://www.moh.gov.om/ email:webmaster@moh.gov.om
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients who give informed consent; 2. Patients of either sex with age ≥18; 3. ASA physical status I or II; 4. Patients undergoing General Anesthesia for elective ambulatory surgery and sutaible for supraglottic device placement.

Exclusion criteria

Exclusion criteria: 1. Predictors of or a history of difficult intubation; 2. Immobilized cervical spine; 3. A history of uncontrolled gastroesophageal reflux or hiatus hernia; 4. Any pathologies of the mouth, pharynx or larynx, the access to the airway is restricted, or a difficult tracheal intubation is anticipated.

Design outcomes

Primary

MeasureTime frame
Successful placement of PLM in first two attempts or records it as failure.

Secondary

MeasureTime frame
1. Time to place PLM in seconds (start of introduction to first adequate capnographic curve); 2. Ease of placement of GT (Easy [E], Difficult [D] or Failed [F]); 3. On removal of the device, any visible evidence of blood on the PLM (Y= yes, N= no); 4. Pre-induction HR & MAP and at 1, 5 &10 min after insertion of device.

Contacts

Public ContactNaresh Kaul

PO Box 514

naresh.kumar@moh.gov.om

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)