Does NoL-monitoring influence the intraoperative opioid requirement during da Vinci-prostatectomies?

Not Applicable

• Conditions: R52.0; Acute pain

• Registration Number: DRKS00023232
• Lead Sponsor: Technische Universität Dresden Universitätsklinikum Carl Gustav Carus Klinik und Poliklinik für Anästhesiologie und Intensivtherapie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-11-03
• Study Completion: 2021-02-10
• Results First Posted: 2022-05-25
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: Male
• Target Recruitment: 50

Inclusion Criteria

Male, da Vinci-Prostatectomie, sinus rhythm

Exclusion Criteria

Cardiac arrhythmia, non legal competent adult, missing consent

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sufentanil administration intraoperativ

Secondary Outcome Measures

Name	Time	Method
RS postoperative, Nausea postoperative