Postoperative Pain Monitoring With ANI in Lumbar Spine Surgery
Recruiting
N/A
Interventional Study
Postoperative Pain
Lumbar Spine Surgery
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 100 (estimated)
- Sponsor
- Akdeniz University Hospital · Other
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About This Trial
This study aims to compare two different pain management methods in patients undergoing elective lumbar spine surgery. Patients are randomly assigned to receive either an ultrasound-guided erector spinae plane block (ESPB) or intravenous multimodal analgesia.
Postoperative pain will be assessed using both clinical pain scores and the Analgesia Nociception Index (ANI), a non-invasive monitoring sy…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age between 18 and 65 years
* ASA physical status I-II
* Scheduled for elective lumbar spine surgery
* Ability to provide informed consent
Exclusion Criteria:
* Known allergy to study medications
* Coagulation disorders
* Infection at the block site
* Severe cardiovascular d…
Contacts