Comparison of Goal-directed Analgesia Using ANI (Analgesia/Nociception Index) and Standard Analgesia During General Anesthesia in Patients Undergoing Orthognathic Surgery on Postoperative Quality of Recovery: a Prospective Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to determine whether goal-directed analgesia using ANI(Analgesia/Nociception Index) can improve the quality of postoperative recovery in patients undergoing maxillofacial surgery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adult patients 18 or older undergoing maxillary, mandibular, or bimaxillary surgery under general anesthesia.

• adult patients who can provide written informed consent to participate in the study, understand the procedures of this study, and be able to complete patient-reported questionnaires adequately.

• adult patients who Have made an informed decision to participate in this study and have given written consent.

Locations
Other Locations
Republic of Korea
Seoul National University Children's Hospital
RECRUITING
Seoul
Time Frame
Start Date: 2024-01-25
Estimated Completion Date: 2026-12-30
Participants
Target number of participants: 86
Treatments
Experimental: goal-directed analgesia using ANI monitoring
Active_comparator: Standard monitoring
Related Therapeutic Areas
Sponsors
Leads: Seoul National University Hospital

This content was sourced from clinicaltrials.gov