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A study of analgesic nociception index-guided requiring a dose of remifentanil during mechanical ventilatory support under continuous sedation in the intensive care unit

A study of analgesic nociception index-guided requiring a dose of remifentanil under continuous sedation in the intensive care unit - A study of analgesic nociception index-guided requiring a dose of remifentanil during mechanical ventilatory support under continuous sedation in the intensive care unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000051696
Enrollment
60
Registered
2023-08-01
Start date
2023-08-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Postoperative patients required mechanical ventilatory support under continuous sedation in the intensive care unit

Interventions

During the surgery, the required dose of fentanyl is determined by the individual responsible anesthesiologist. The dose of fentanyl may probably be adjusted within the range of effect-site concentrat

Sponsors

Ehime university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Postoperative patients required mechanical ventilatory support under a continuous infusion of sedative agents in intensive care until the next morning. The elective surgeries enrolled in this study are as followed, tumor resection and reconstruction by surgeons of otolaryngology or dental surgery or plastic surgery, upper and lower jaw migration by dental surgeons, and thoracoscopic esophageal malignancy surgery.

Exclusion criteria

Exclusion criteria: Patients are 18 years old or less, have severe arrhythmia, atrial fibrillation, and an implanted pacemaker, require high doses of catecholamines, or take some opioid medications preoperatively.

Design outcomes

Primary

MeasureTime frame
The total dose of remifentanil administered between admission to the intensive care unit and eight hours after admission

Secondary

MeasureTime frame
The mean score of HFVI, the Total dose of sedative agents, the frequency of analgesics required after the termination of mechanical ventilatory support, the VAS score after the termination of mechanical ventilatory support, and the development of delirium after the termination of mechanical ventilatory support

Countries

Japan

Contacts

Public ContactYukihiro Nakasaki

Ehime University Hospital Division of Intensive care unit

yukihiro.nakata.zd@ehime-u.ac.jp0899605383

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026