Intraoperative Analgesia Nociception Index (ANI) in elderly patients during Hip surgery: a randomized clinical trial.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0007697

Enrollment

Registered

2022-09-16

Start date

2022-06-30

Completion date

Unknown

Last updated

2022-10-24

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

Conditions

None listed

Interventions

Medical Device : We compare the total dose of remifentanil used during surgery between the group to which the ANI monitor was applied and the control group to which only a general hemodynamic monitor

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The patients scheduled for hip surgery, ASA I~III

Exclusion criteria

Exclusion criteria: Patients with planned regional anesthesia such as spinal/epithelial anesthesia, patients who underwent nerve block for pain control, with BMI 35 kg/m2 or more, with baseline MBP less than 60 mmHg, with baseline heart rate less than 45 bpm/120 bpm , patients on chronic opioid medications, arrhythmias, patients on implanted pacemaker, patients taking alpha 2 adrenergic agonists, beta 1 adrenergic antagonists, antiarrhythmic agents, patients with central/autonomous nervous system disorder

Design outcomes

Primary

Measure	Time frame
intraoperative remifentanil total dose	—

Secondary

Measure	Time frame
the adverse event due to opioid use	—

Countries

Korea, Republic of

Contacts

Public ContactHeo Min Hee

Inje University Ilsan Paik Hospital

mini0603@hanmail.net+82-31-910-7157

Outcome results