Remifentanil use for procedural sedation and analgesia in the emergency department

Albert Schweitzer hospital, Dordrecht, The NetherlandsM.A.A. van Hooft 0 sites60 target enrollmentTBD

Conditionsremifentanil, target controlled infusion, procedural sedation, analgesia, recovery time, emergency department, propofol, fentanyl.procedurele sedatie, pijnstilling, hersteltijd, spoedeisende hulp.

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: remifentanil, target controlled infusion, procedural sedation, analgesia, recovery time, emergency department, propofol, fentanyl.procedurele sedatie, pijnstilling, hersteltijd, spoedeisende hulp.
Sponsor: Albert Schweitzer hospital, Dordrecht, The NetherlandsM.A.A. van Hooft
Enrollment: 60
Status: Recruiting
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

TBD

End Date

TBD

Last Updated

2 years ago

Study Type

Interventional

Investigators

Sponsor

Albert Schweitzer hospital, Dordrecht, The NetherlandsM.A.A. van Hooft

Eligibility Criteria

Inclusion Criteria

•All the patients who need procedural sedation and analgesia at the emergency department or the observatorium of the Albert Schweitzer hospital location Dordwijk in Dordrecht, age 18 years and older, classified as ASA I en II.

Exclusion Criteria

•Age under 18 years, hemodynamic and/or respiratory instable, classified as ASA III, IV and V, suspicion of elevated intra\-cranial pressure, pregnancy, use of opiates at home, opiates administered before PSA procedure started (in the ambulance, on arrival at the emergency department), intoxication, known allergy for fentanyl propofol remifentanil soy or chicken proteins.

Outcomes

Primary Outcomes

Not specified

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