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Comparing Skin Conductance and Nol-index

F

Free University of Brussels (ULB)

Status

Unknown

Conditions

Cardiac Disease
Analgesia
Vascular Diseases
Monitoring
Anesthesia

Treatments

Device: Skin Conductance
Device: Nol-Index

Study type

Observational

Funder types

Other

Identifiers

NCT04138966
P2019/427Am1

Details and patient eligibility

About

Comparison of twà different nociception monitors during general anesthesia

Full description

Analgesia remains a challenge in anesthesia. Several monitors have shown potential in detecting insufficient analgesia during general anesthesia, but they have not been investigated in patients undergoing cardiac and vascular surgery. In this study, we will compare skin conductance (Medstorm, Norway) and nol-index (Medasense, Israel) w during noxious and non-noxious stimuli. This study is carried out on patients included in another study (Nol-Index Guided Remifentanil Analgesia Versus Standard Analgesia During Moderate-to-High Risk Cardiovascular Surgery).

Enrollment

10 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • moderate-to-high risk cardiac or vascular surgery
  • ASA 2-4

Exclusion criteria

  • chronic arrhythmia (e.g. atrial fibrillation)
  • aortic insufficiency
  • pacemaker
  • implanted defibrillator
  • valve surgery

Trial design

10 participants in 1 patient group

Patients undergoing general anesthesia
Description:
Patients are monitored with Nol-Index, skin conductance, and antinociception-index
Treatment:
Device: Nol-Index
Device: Skin Conductance

Trial contacts and locations

1

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Central trial contact

Luc Barvais, MD, PhD; Sean Coeckelenbergh, MD

Data sourced from clinicaltrials.gov

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