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Steroid Treatment to Prevent Thoracic Endovascular Aortic Repair Postimplantation Syndrome
Sponsor: University of Belgrade
Summary
Postimplantation syndrome (PIS) is a common and clinically important complication following thoracic endovascular aortic repair (TEVAR). PIS is characterized by a strong systemic inflammatory response to the stent-graft implantation and is manifested by flu-like symptoms, which include fever, increased white blood count, increased levels of acute phase proteins, and fatigue, but without a clear inflammatory and infective cause. Besides, it has been demonstrated that PIS is associated with prolonged hospital stay and increased risk for postoperative complications, including acute kidney injury, postoperative delirium, and increased postoperative pain scores. Recently, there has been increasing evidence that PIS is associated with an increased risk of major adverse cardiac events (MACE) and perioperative myocardial injury. Observational studies suggest that preoperative administration of glucocorticoids may decrease the incidence of PIS after TEVAR and EVAR procedures. However, to date, there are no randomised trials that have investigated whether preoperative administration of glucocorticoids can reduce the incidence of PIS and its associated poorer treatment outcomes following TEVAR. This randomized controlled trial was designed to investigate the effect of glucocorticoid administration on reducing the incidence and improving the outcome of patients who develop PIS after TEVAR.
Official title: Steroid Treatment to Prevent Thoracic Endovascular Aortic Repair Postimplantation Syndrome (STOP TEVAR PIS): A Randomized, Double-Blind, Placebo-Controlled Trial
Key Details
Gender
All
Age Range
18 Years - 90 Years
Study Type
INTERVENTIONAL
Enrollment
174
Start Date
2026-01
Completion Date
2029-01
Last Updated
2026-01-12
Healthy Volunteers
No
Interventions
Methylprednisolone (MP)
Patients in the MP group would receive 30 mg/kg of methylprednisolone, dissolved in 100 mL of saline, via a 30-minute slow intravenous infusion.
Placebo (saline)
Patients randomized to the placebo group would receive 100 mL of physiological solution two hours prior to the intervention.
Locations (1)
Clinic for Vascular and Endovascular Surgery, University Clinical Center of Serbia
Belgrade, Serbia