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Evaluation of different positive end-expiratory pressures using Supreme™ Airway laryngeal mask during minor surgical procedures in children

Evaluation of different positive end-expiratory pressures using Supreme™ Airway laryngeal mask during minor surgical procedures in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00013254
Enrollment
71
Registered
2017-11-27
Start date
2012-01-19
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

lung recruitment, aspiration of gastric air

Interventions

Group 1: We conducted this prospective clinical trial over a period from February 2012 to August 2014. We included children aged between 1 and 12 years old, who were scheduled for an elective inguinal

Sponsors

Universitätsmedizin MannheimKlinik für Anästhesie und operative Intensivmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Months to 12 Years

Inclusion criteria

Inclusion criteria: We included children aged between 1 and 12 years old, who were scheduled for an elective inguinal hernia repair or circumcision, with general anaesthesia using a laryngeal mask. In addition, allocation to the American Society of Anaesthesiologists (ASA) classification I-III was a prerequisite for participation. Inclusion of patients was after informed consent.

Exclusion criteria

Exclusion criteria: Exclusion criteria were an ASA classification IV and above, children with difficult airways or impossibility of insertion of the laryngeal mask or the gastric tube.

Design outcomes

Primary

MeasureTime frame
Primary outcome parameters were changes of the dynamic compliance and end-tidal carbon dioxide (etCO2) to verify recruitment maneuver’s with PEEP in lungs. We did three different measurements on three PEEP levels (T0 PEEP 5, T1 PEEP 3, T2 PEEP 0).

Secondary

MeasureTime frame
Secondary outcome parameters were the gastric air insufflation during ventilation with three different PEEP levels.

Countries

Germany

Contacts

Public ContactElke Thiel

Universitätsmedizin Mannheim

elke.thiel@umm.de0621-383-3536

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026