NCT06336161

Comparison Between Ultrasound-Guided Erector Spinae Plane Block Versus Ultrasound-Guided Caudal Injection

Comparison Between Ultrasound-Guided Erector Spinae Plane Block Versus Ultrasound-Guided Caudal Injection in Lumbosacral Spine Surgeries for Postoperative Pain Management
Al-Azhar University·ClinicalTrials.gov·drugNot yet recruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Postoperative Pain
Drug/Device/Intervention
Fentanyl
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Al-Azhar University
Location
Cairo, Egypt
Timeline & enrollment
Phase
N/A
Start date
Apr 01, 2024
End date
May 01, 2025
Enrollment
80 participants
Primary outcome

Measurement of Post-operative Pain

Summary

Patient-controlled analgesia is typically used to relieve postoperative pain.
 Patient-controlled analgesia, on the other hand, is prone to opioid-related side effects.
 Furthermore, standard postoperative analgesia has a limited analgesic impact. If
 postoperative lumbosacral spine pain is not successfully treated, it can progress to chronic
 pain, compromising patients' quality of life.
 
 The methods of access for epidural injections are characterized as transforaminal,
 interlaminar, or caudal. Caudal epidural injections (CEI) are often utilized as a diagnostic
 or therapeutic tool in a range of lumbosacral-originating spinal pain problems, and they are
 especially useful in patients with complicated lumbar epidural access diseases, such as post
 laminectomy syndrome. It is regarded as a very simple treatment in the realm of
 interventional pain management, and it is also recognized to have a reduced risk of
 inadvertent Dural puncture than other epidural techniques

ICD-10 classifications
Acute painPostoperative intestinal obstructionPain, unspecifiedDuring surgical operationDuring surgical operation
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06336161
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06336161 through Pure Global AI's free database. This phase not specified trial is sponsored by Al-Azhar University and is currently Not yet recruiting. The study focuses on Postoperative Pain. Target enrollment is 80 participants.

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