Comparison of the effects of anesthesia using remifentanil and standard anesthesia using the analgesic index during remimazolam anesthesia.

Analgesia Nociception Index-Guided Remifentanil versus Standard Care during Remimazolam Anesthesia: A Randomized Controlled Trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0008999

Enrollment

Registered

2023-11-30

Start date

2023-12-01

Completion date

Unknown

Last updated

2023-12-19

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

Conditions

None listed

Interventions

Drug : Upon entering the operating room, both groups will have an electrocardiogram, non-invasive blood pressure monitor, pulse oximeter, and esophageal thermometer. To evaluate the depth of sedation,

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Relevant patient conditions ? American Society of Anesthesiologists physical classification I, II or III ? Patients who agreed to participate in the study among patients over 18 years old and under 80 years old ? Patients undergoing laparoscopic lower gastrointestinal surgery performed at our Hospital

Exclusion criteria

Exclusion criteria: 2) Patient exclusion conditions ? Outpatient and emergency surgery ? People who are in the intensive care unit or who are scheduled to be transferred to the intensive care unit after surgery ? Patients with morbid obesity (BMI>30) ? Mother or lactating woman ? People with Child-Turcotte-Pugh Class C liver function abnormalities ? Patients with chronic pain for more than 3 months ? Patients with arrhythmia or pacemaker holders ? People who regularly take beta blockers ? People who are unable to communicate and have cognitive impairment ? People who cannot understand the consent form

Design outcomes

Primary

Measure	Time frame
intraoperative remifentanil consumption	—

Secondary

Measure	Time frame
intraoperative ANI change;Changes in vital signs during intraoperative and postoperative period;Changes in the depth of sedation during intraoperative and postoperative period;Whether to use atropine or ephedrine during and after alcohol;Changes in intraoperative target blood concentration of remifentanil;time required to awakening after cessation of sedation;Post-operative VAS score;Total PCA usage;use of additional painkillers;postsedative nausea and vomiting;urinary retention;hospital stay dates	—

Measure

Time frame

intraoperative ANI change;Changes in vital signs during intraoperative and postoperative period;Changes in the depth of sedation during intraoperative and postoperative period;Whether to use atropine or ephedrine during and after alcohol;Changes in intraoperative target blood concentration of remifentanil;time required to awakening after cessation of sedation;Post-operative VAS score;Total PCA usage;use of additional painkillers;postsedative nausea and vomiting;urinary retention;hospital stay dates

—

Countries

Korea, Republic of

Contacts

Public ContactSung haeng Kim

Dong-A University Hospital

hang930415@gmail.com+82-51-240-5390

Outcome results