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Comparing the effects of applying a multimodal analgesic strategy including cervical plexus block to improve postoperative pain management in patients undergoing carotid endarterectomy: a randomized, observer-blinded trial

Comparing the effects of applying a multimodal analgesic strategy including cervical plexus block to improve postoperative pain management in patients undergoing carotid endarterectomy: a randomized, observer-blinded trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008461
Enrollment
40
Registered
2023-05-23
Start date
2023-05-24
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

None listed

Interventions

Procedure/Surgery : In the control group, at the end of the surgery, the surgeon performs a superficial CPB method of injecting local anesthetic ropivacaine into the subcutaneous tissue around the sur

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult patients undergoing elective carotid endarterectomy under general anesthesia (aged between 20 and 80 years of age) 2. American Society of Anesthesiologists (ASA) physical status classification (ASA class) I- III 3. A person who consented to the clinical trial and signed the subject consent form

Exclusion criteria

Exclusion criteria: 1. Children under the age of 19, adults over the age of 80 2. Patients who refused cervical plexus block 3. Patients with neurological abnormalities 4. Patients with bleeding abnormalities or disabilities 5. Those who cannot undergo nerve block surgery due to recent systemic or partial infection 6. Patients who have taken opioids for a long time, patients with a history of severe side effects to opioids 7. Patients allergic to local anesthetics 8. A person who is judged to be inappropriate to participate in a clinical trial according to the judgment of the researcher 9. Patients with a history of previous CEA surgery 10. Patients who have failed cervical plexus block

Design outcomes

Primary

MeasureTime frame
Total Intravenous morphine equivalent for 24 hours after surgery

Secondary

MeasureTime frame
Pain score in ICU at rest after surgery;Pain score when moving after surgery in the intensive care unit;Time of first narcotic analgesic administration after surgery;Frequency of hypertension (defined: systolic blood pressure >140 mmHg) 24 hours after surgery;Use of antihypertensive drugs (hydralazine) within 24 hours after surgery;Frequency of nausea or vomiting within 24 hours after surgery;Satisfaction with pain control after surgery;Sleep satisfaction on the first night after surgery;24-hour postoperative recovery questionnaire score;Frequency of postoperative complications (hoarseness, neurologic complication, recurrent laryngeal nerve block);cerebral hyperperfusion syndrome ;Intraoperative analgesia nociception index (ANI) score

Countries

Korea, Republic of

Contacts

Public ContactJISUN CHOI

Samsung Medical Center

luck8909@naver.com+82-2-3410-2470

Outcome results

None listed

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