Efficacy and Safety of Preemptive Intravenous Dexamethasone in MIS-TLIF

Recruiting Phase 4 Interventional Study
Spinal Stenosis Lumbar Disc Degeneration Disc Disease Fusion of Spine Surgery
Prior Safety Data This treatment has already been tested in at least one earlier human trial. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
50 – 80
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
60 (estimated)
Sponsor
Potsawat Surabotsopon · Other
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About This Trial

Researchers are considering Dexamethasone as preemptive medication before minimally invasive spine fusion surgery to minimize postoperative back pain with minimal side effects, aiming to enhance the effectiveness of surgery and improve patient outcomes.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age range: 50-80 years old. * Undergoing MIS TLIF surgery at 1-2 spinal levels. Exclusion Criteria: * Previously undergone spine surgery. * HbA1C greater than or equal to 7.5 mg% * Allergic to all types of experimental medication. * History of using systemic steroids.
Contacts

Konthorn Chankong, Master's degree

+66859496902

gearkonthorn@gmail.com

CONTACT