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Pterygopalatine Fossa Block in Aneurysmal Subarachnoid Hemorrhage

The University of Texas System (UT) logo

The University of Texas System (UT)

Status and phase

Completed
Early Phase 1

Conditions

Subarachnoid Hemorrhage, Aneurysmal

Treatments

Drug: Bupivacaine 0.25% Injectable Solution
Procedure: Ptergyopalatine Fossa Block

Study type

Interventional

Funder types

Other

Identifiers

NCT05925478
STU-2023-0176

Details and patient eligibility

About

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.

Enrollment

2 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aneurysmal subarachnoid hemorrhage with secured aneurysm
  • Age greater than or equal to 18 years
  • Able to communicate pain level

Exclusion criteria

  • Documented allergy to local anesthetics (e.g. bupivicaine)
  • Patients with unsecured aneurysms
  • Patients who are unable to communicate pain level (e.g. sedation/mechanical ventilation/delirium, etc)
  • Medical treatment for vasospasm including blood pressure/inotropic augmentation
  • Angiographic treatment for vasospasm within 48 hours

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

2 participants in 1 patient group

Treatment arm
Experimental group
Treatment:
Procedure: Ptergyopalatine Fossa Block
Drug: Bupivacaine 0.25% Injectable Solution

Trial contacts and locations

1

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Central trial contact

Noah Jouett, DO/PhD

Data sourced from clinicaltrials.gov

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