Prospective Randomized Observer Blinded Single Center Study Comparing 90-day Functional Outcome in Patients Who Received Intravenous Propofol Infusion Versus Inhalational Sevoflurane for General Anesthesia During Mechanical Thrombectomy in Patients Who Suffered From Acute Ischemic Stroke
Recruiting now · Not applicable
Conditions studied: Acute Ischemic Stroke Patients
In brief
This study is being done to compare outcomes after surgery for individuals who receive anesthesia through by inhaling medication and individuals who receive anesthesia intravenously by needle when experiencing treatment for their stroke. Currently very little is known about the outcomes for patients when comparing these two techniques of providing anesthesia during surgery. This study will provide information regarding outcomes that will help health care providers decide which technique will be better for patients
Key facts
- Study ID
- NCT07001267
- Run by
- University of Kansas Medical Center
- People needed
- 120
- Starts
- 2025-06-04
- Expected to finish
- 2027-12-31
- Last updated by the study team
- 2026-03-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- >18 years Acute ischemic stroke requiring endovascular treatment.
You may not qualify if…
- <18 years
- Pregnant patients
- Patients with malignant hyperthermia
- Allergies or any contraindications to either inhalational or intravenous agents
- Patients already on intravenous anesthetic infusions
- Prisoners
- Students and employees
Where it is running
- University of Kansas Medical Center — Kansas City, Kansas, United States (enrolling)
Full record on ClinicalTrials.gov
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