CVI BIS study.
Recruiting
- Conditions
- In the current study we will measure CVI as a measure of adequate analgesia in ASA 1-3 patients during elective abdominal surgery under fentanyl/sevoflurane/epidural anesthesia. We will monitor patient movement as primary correlate to CVI and cardiovascular parameters as secondary correlates (eg, cardiac output, pulse transit time, blood pressure and heart rate).
- Registration Number
- NL-OMON24098
- Lead Sponsor
- eiden University Medical Center, dept of Anesthesiology
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1. Age: 18-80 years;
2. Sex: Male or female;
Exclusion Criteria
1. Age: < 18 or > 80 years;
2. Unable to give written informed consent;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method We will monitor patient movement and corresponding CVI & BIS values as a measure of adequate pain relief during surgery.
- Secondary Outcome Measures
Name Time Method Any change in cardiovascular variables. Cardiovascular monitoring will include: Pulse transit time (PTT), heart-rate, blood pressure and cardiac output as calculated from the arterial pressure pulse wave.