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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Ptergyopalatine Fossa Block | Injection of local anesthetic (e.g. Bupivacaine) into the pterygopalatine fossa to treat headache related to aneurysmal subarachnoid hemorrhage |
| DRUG | Bupivacaine 0.25% Injectable Solution | Injection 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05925478. Inclusion in this directory is not an endorsement.