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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06157762
Other study ID # 2022/26-05
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date December 2023
Est. completion date October 2024

Study information

Verified date November 2023
Source Kahramanmaras Sutcu Imam University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Erector spinae plane (ESP) block is an interfacial plane block with visceral and somatic analgesic activity at paraspinal muscles.ESPB has been successfully applied as a part of multimodal analgesia in treating postoperative pain in spinal surgery. However, it may be difficult or impossible to perform lumbar ESPB in obese patients or cases of increased lumbar lordosis. This study aims to investigate the effectiveness of ESPB applied by the intraoperative surgeon.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 56
Est. completion date October 2024
Est. primary completion date October 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - ASA I-III patients - Agreed to participate in the study Exclusion Criteria: - Patients with infection at the injection site - Coagulopathy Allergy to amide-type local anesthetics - History of peripheral neuropathy - Hepatic and/or renal failure - Refusing the procedure - Patients with heart disease - Patients who have previously undergone surgery from the same area

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Erector spinae plane block
ultrasound guided lumbar erector spinae plane block
Erector spinae plane block performed by surgeon
Erector spinae plane block performed by surgeon

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Kahramanmaras Sutcu Imam University

Outcome

Type Measure Description Time frame Safety issue
Primary opioid consumption The amount of morphine consumed in milligrams in the first 24 hours was determined with a patient-controlled analgesia pump. up to 24 hour
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