Overview

Acetazolamide Challenge With Perfusion in the Prediction of Cerebral Vasospasm

Status:
Recruiting
Trial end date:
2022-12-01
Target enrollment:
0
Participant gender:
All
Summary
The investigators propose a technique using cone beam CT perfusion (CBCTP) imaging with an acetazolamide challenge as a potential diagnostic tool to detect a defect in cerebral autoregulation at a time when it has not yet caused clinically apparent signs or symptoms. 30 participants will be enrolled at the University of Wisconsin - Madison and can expect to be on study for about 2 weeks.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Wisconsin, Madison
Treatments:
Acetazolamide
Criteria
Inclusion Criteria:

- Patients with aneurysmal subarachnoid hemorrhage presenting to our institution within
24 hours of symptom onset

- Adults, 18 years of age or older

- Women of childbearing potential must not be pregnant (negative urine pregnancy test)

Exclusion Criteria:

- Contraindication to acetazolamide (i.e. sulfonamide allergy, renal or liver failure)

- Contraindication to contrast media (Allergy or abnormal serum Cr and/or GFR based on
current UW guidelines for IV contrast)

- Renal insufficiency, history of renal failure or renal transplant

- Hunt and Hess grade 1 and 5 (Attached protocol provides details on the grading scale.
Grade 1 have lowest yield for vasospasm and Grade 5 are by definition critically ill
and unstable patients)

- Critically ill patients who are unstable and who cannot undergo scans within the
proposed timeline i.e. within 24 hours of the onset of their symptoms.