Clinical Trials Directory

Trials / Completed

CompletedNCT05925478

Pterygopalatine Fossa Block in Aneurysmal Subarachnoid Hemorrhage

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
2 (actual)
Sponsor
University of Texas Southwestern Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Aneurysmal subarachnoid hemorrhage (aSAH) can cause a severe headache (HA) that is famously treatment-resistant. Current pain regimens are too reliant on opioids, which results in long-term opioid dependence and can obfuscate the neurological examination, which is critical to detect vasospasm and delayed cerebral ischemia. This study will gather the initial evidence of whether the pterygopalatine fossa (PPF) regional anesthesia nerve block can treat aSAH-related HA and reduce opioid consumption in patients with aSAH.

Conditions

Interventions

TypeNameDescription
PROCEDUREPtergyopalatine Fossa BlockInjection of local anesthetic (e.g. Bupivacaine) into the pterygopalatine fossa to treat headache related to aneurysmal subarachnoid hemorrhage
DRUGBupivacaine 0.25% Injectable SolutionInjection of local anesthetic (e.g. Bupivacaine) into the pterygopalatine fossa to treat headache related to aneurysmal subarachnoid hemorrhage

Timeline

Start date
2023-11-06
Primary completion
2024-08-20
Completion
2024-08-20
First posted
2023-06-29
Last updated
2024-08-22

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05925478. Inclusion in this directory is not an endorsement.