Support of pain therapy by continuous algesia measurements by A.N.I. monitor in postoperative patients at the recovery room

Not Applicable

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

• Registration Number: DRKS00006220
• Lead Sponsor: niversitätsklinikum Aachen Klinik für Anästhesiologie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-07-16
• Study Completion: 2016-07-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 138

Inclusion Criteria

1.not less than 18 years old, capable of giving consent
2.painful operative intervention, calculated minimum duration of 90 minutes
3.general anesthesia
4.planned postoperative stay in recovery room

Exclusion Criteria

beta blockers, cardiac pacemakers/ICD, catecholamine therapy, periduralcatheter (PDK), PCA pump (patient controlled analgesia), arrhythmias, bradypnea <9/min, heart transplant

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
umeric Rating Score (average point value), measured pain intensity

Secondary Outcome Measures

Name	Time	Method
Quantity of pain occurrence described by the patient during his stay in the recovery room, satisfaction of the patient (questionnaire after leaving the recovery room), duration of stay in the recovery room, total dose of applicated analgesics, incidence of adverse events in the recovery room (nausea, vomit, hypotension, hypertension, tachycardia, bradycardia), Aldrete-Score (charged every 15min), „Surgical Stress index (SSI)