EEG-derived pain threshold index guided versus standard care during Remifentanil-Propofol Anesthesia

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100045011

Enrollment

Unknown

Registered

2021-04-03

Start date

2021-04-06

Completion date

Unknown

Last updated

2021-11-08

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

Conditions

Abdominal operation

Interventions

Experimental group:EEG-derived pain threshold index-guided

Control group:Standard care

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Signed Informed Consent; 2. Age between 18 and 65 years old; 3. ASA classification I-III; 4, 18 < BMI < 30; 5. No serious cardiac diseases, serious pulmonary diseases and other important organ dysfunction; 6. Patients who are scheduled to receive abdominal surgery.

Exclusion criteria

Exclusion criteria: 1. Preoperative use of opioid drugs or non-opioid drugs for analgesia; 2. Patients with history of chronic pain before surgery; 3. Patients with a history of central nervous system; 4. Preoperative use of anticholinergic/cholinergic drugs; 5. Intraoperative spinal anesthesia or other local analgesia is planned; 6. Patients with acute pain before surgery.

Design outcomes

Primary

Measure	Time frame
Remedial analgesia rate;	—

Secondary

Measure	Time frame
Dosage of remedial analgesics;Pain intensity;Amount of remifentanil used during operation;	—

Countries

China

Contacts

Public ContactLiu Xuesheng

Department of Anesthesiology, the First Affiliated Hospital of Anhui Medical University

liuxuesheng@ahmu.edu.cn+86 18655193385

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026