Effect of duration of procedural sedation on postprocedural respiration

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON21394

Enrollment

100

Registered

2020-01-24

Start date

2020-01-23

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

Atelectasis, upper respiratory tract infections

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: o Planned for procedure under PSA performed by the department of anesthesiology o Passed screening for PSA o Procedure will potentially last longer than 2 hours o Procedure performed in prone position o SpO2 on room air pre-procedurally > 96%

Exclusion criteria

Exclusion criteria: o Procedure with prolonged esophageal or bronchial manipulation o ASA status IV o COPD Gold 3-4 o previous lung surgery o use of CPAP for OSAS o Use of FiO2 > 50% during procedure o Use of endotracheal intubation during procedure o Use of Optiflow during procedure o need for additional bolusses of esketamine during the procedure

Design outcomes

Primary

Measure	Time frame
Atelectasis after procedural sedartion	—

Secondary

Measure	Time frame
Signs and symptoms of upper respiratory tract infections	—

Contacts

Public ContactClemens Barends

University Medical Center Groningen

c.r.m.barends@umcg.nl050-3616161

Outcome results