Sevoflurane/fentanyl anesthesia guided by Nociceptive-Level index during abdominal surgery in ASA 1-3 patients * a randomized controlled trial on the effect of NOL-guidance on postoperative pain scores

Sevoflurane/fentanyl anesthesia guided by Nociceptive-Level index during abdominal surgery in ASA 1-3 patients * a randomized controlled trial on the effect of NOL-guidance on postoperative pain scores - SOLAR

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON48484

Enrollment

Registered

2019-03-12

Start date

2019-06-20

Completion date

Unknown

Last updated

2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

perioperatieve patienten anesthesia pain

Interventions

NOL-guided versus standard of care anesthesia

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 years and older; 2. ASA I-II-III 3. Elective surgery

Exclusion criteria

Exclusion criteria: 1. Unable to give written informed consent; 2. Use of epidural analgesia or local anesthesia (eg. transversus abdominal plain block, TAP block) 3. Non-elective surgery 4. Pregnancy/lactation. 6. Uncontrolled preoperative hypo- or hypertension (Mean arterial pressure 160 mmHg) 7.Preoperative Heart rate 90/min; 8. Central nervous system disorder (neurologic/head trauma/uncontrolled epileptische aanvallen);

Design outcomes

Primary

Measure	Time frame
Postoperartive pain	—

Secondary

Measure	Time frame
Opioid and propofol consumption in total dose and dose/min; and Incidence (number of episodes) of inadequate anesthesia (as derived from heart rate, blood pressure, BIS values)	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)