Assistance of pain treatment through a continuous algesia-measurement for postoperative patients in the recovery room

Not Applicable

• Conditions: postoperative pain; R52.9; Pain, unspecified

• Registration Number: DRKS00000755
• Lead Sponsor: niversitätsklinikum AachenKlinik für Anästhesiologie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2011-04-11
• Study Completion: 2011-06-10
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 44

Inclusion Criteria

at least 18 years
competent
surgical procedure, at least scheduled for 90 min.
OP classification at least III
general anaesthesia
postoperative stay in the recovery room

Exclusion Criteria

beta blocker,
ICD/ pacemaker,
current catecholamines,
epidural catheter,
PCA pump

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
mean numeric rating score given by the patient

Secondary Outcome Measures

Name	Time	Method
umber of pain events during the stay in the recovery room (RR), patient sastisfaction (questionaire after discharge of the RR), duration of stay in the RR, total dose of applicated analgetics (substance and dosis), incidence of side effects (nausea, vomitus, hypotension, hypertension, tachycardia, bradycardia), Aldrete score (each 15 min), salivatory cortisol level (at the beginning and the end of RR stay)