Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT07199816

Pain Control With Caudal Epidural vs. Combined Caudal Epidural and Lumbar Sympathetic Block .

The Analgesic Effect of Caudal Epidural Versus Combined Lumbar Sympathetic Block With Caudal Epidural in Patients Undergoing Redo Lumbar Surgery: A Randomized Double Blinded Controlled Trial.

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
64 (estimated)
Sponsor
Hebatullah Mohammed Abdelmageed · Academic / Other
Sex
All
Age
40 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Comparing the analgesic effect of caudal epidural versus combined lumbar sympathetic block with caudal epidural in patients undergoing redo spinal surgery.

Detailed description

To evaluate the improvement in pain score using numerical rate scale (NRS) over 4 months and compare this between the two groups. * To assess and compare the improvement of motor activity and early ambulation using EuroQo lmeasure (EQ-5D) between the two groups. * To evaluate and compare the overall patient satisfaction between the two groups.

Conditions

Interventions

TypeNameDescription
PROCEDUREFluoroscopy-Guided Caudal Epidural BlockUnder fluoroscopic guidance, the patient in the prone position will receive a caudal epidural injection through the sacral hiatus. A 22-gauge, 3.5-inch spinal needle (Spinocan®, BRAUN) is used to inject 1 mL of contrast media (Omnipaque 300) to confirm correct needle placement. Then, 10 mL of treatment solution (8 mL of 0.5% lidocaine and 2 mL of 8 mg dexamethasone) is administered.
PROCEDURECombined Lumbar Sympathetic Ganglion Block and Caudal Epidural BlockPatients will receive both a caudal epidural block and a lumbar sympathetic ganglion block (LSGB) under fluoroscopic guidance. The LSGB is performed at the L2 or L3 vertebral body on the affected side using a 21-gauge Chiba needle. After confirming needle position with contrast imaging, 10 mL of solution (2 mL of 8 mg dexamethasone + 8 mL of 1% lidocaine) is injected. A caudal block is then performed as described above.

Timeline

Start date
2025-06-01
Primary completion
2026-06-20
Completion
2026-08-01
First posted
2025-09-30
Last updated
2025-09-30

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07199816. Inclusion in this directory is not an endorsement.