Geneva, Oct. 21 -- International Clinical Trials Registry received information related to the study (TCTR20251007013) titled 'Efficacy of Preoperative Single Intravenous Dexamethasone to Reduce Postoperative Pain in Biportal Endoscopic Transforaminal Interbody Fusion' on Oct. 7.
Study Type: Interventional
Study Design:
Randomized
Primary Sponsor: Rattalerk Arunakul
Condition:
Participants must present with low back pain and/or radiating pain to the lower limbs, and/or neurogenic intermittent claudication that has not responded to appropriate conservative treatment for at least six months.
EndoTLIF
Preemptive dexamethasone
EndoTLIF
Preemptive dexamethasone
Intervention:
Single IV Dexamethasone 0.2 mg/kg group (max dose 12 mg ) inj...