Skip to main content
Clinical Trials/DRKS00012329
DRKS00012329Completed未知

Postoperative time of extubation and incidence of postoperative nausea and vomiting due to intraoperative pupillometry-controlled analgesia - P_AL_EX

Klinik für Anästhesiologie, Intensiv-, Palliativ- und Schmerzmedizin; Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil, Bochum0 sites64 target enrollmentStarted: May 24, 2017Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
64

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomized controlled study
Masking
Blinded (masking used)

Eligibility Criteria

Ages
18 Years to one (—)
Sex
All

Inclusion Criteria

  • voluntariness; preoperative written confirmed consent, elective surgery with use of heart-lung machine or implantation of transapical aortic valve (TAVI), adequate knowledge of the German language, 18 years of age

Exclusion Criteria

  • < 18 years; withdrawal of agreement; employees of the investigator or of the facility that is participating in this clinical research oder other studies; simultaneous participation in an AMG-study; emergency surgery; glass eye; anisocoria, non-treated hypertension, advanced Dibates mellitus HbA1C >8.5%, concomitant treatment with opioids or antidepressants, eye drugs for topical application, psychiatric disorder.
  • Secondary: BDI > 20 points, early postoperative complications, intraopertive injection of atropine, MCP/ DHB, intraopertive hypothermia <32°C.

Investigators

Sponsor
Klinik für Anästhesiologie, Intensiv-, Palliativ- und Schmerzmedizin; Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil, Bochum

Similar Trials

Postoperative time of extubation and... | Clinical Trial