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NOT YET RECRUITING
NCT07328906
NA

Steroid Treatment to Prevent Thoracic Endovascular Aortic Repair Postimplantation Syndrome

Sponsor: University of Belgrade

View on ClinicalTrials.gov

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

DRUG

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.

DRUG

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