Intraoperative measurement of nociception in elective lung surgery by determining the NOL index (PAINOL-trial)

• Conditions: R52.2; R07.3; Other chronic pain; Other chest pain

• Registration Number: DRKS00017798
• Lead Sponsor: Chirurgische Klinik Campus Charité Mitte / Campus Virchow-Klinikum CCM/CVK

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-05-13
• Study Completion: 2022-03-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 180

Inclusion Criteria

elective thoracic surgery
Patient is able to give consent
Age =18 years
signed declaration of consent

Exclusion Criteria

insufficient knowledge of German
non-elective thoracic surgery
Re-Thoracotomies

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Correlation between the under general anesthesia measured parameter Nociception Level Index (NOL) with the intensity of subjective pain perception (NRS, chronic post-thoracotomy syndrome) recorded 6 months postoperatively

Secondary Outcome Measures

Name	Time	Method
Correlation between the during general anesthesia measured nociception level index (NOL) with the postoperative complication rate.<br>