Trials / Unknown
UnknownNCT04138966
Comparing Skin Conductance and Nol-index
Nociceptive Monitoring With Skin Conductance and Nol-index in Moderate-to-high Risk Cardiovascular Patients
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 10 (estimated)
- Sponsor
- Erasme University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- —
Summary
Comparison of twà different nociception monitors during general anesthesia
Detailed 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).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Nol-Index | Multiparametric monitor that studies that establishes an index as a surrogate to nociception |
| DEVICE | Skin Conductance | Measures skin conductance as a surrogate to nociception |
Timeline
- Start date
- 2019-10-20
- Primary completion
- 2020-06-01
- Completion
- 2020-12-20
- First posted
- 2019-10-25
- Last updated
- 2020-11-09
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT04138966. Inclusion in this directory is not an endorsement.