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

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00017798

Enrollment

120

Registered

2020-05-13

Start date

2019-09-05

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

R52.2 R07.3

Interventions

Group 1: elective thoracic surgery: intraoperative NOL-Monitoring (PMD 200 von MEDASENSE), postoperative pain measurement (NRS)

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: insufficient knowledge of German non-elective thoracic surgery Re-Thoracotomies

Design outcomes

Secondary

Measure	Time frame
Correlation between the during general anesthesia measured nociception level index (NOL) with the postoperative complication rate.	—

Primary

Measure	Time frame
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	—

Countries

Germany

Contacts

Public ContactJens Neudecker

Chirurgische Klinik Campus Charité Mitte / Campus Virchow-Klinikum CCM/CVK

jens.neudecker@charite.de+49 30 450 552 001

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026