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NCT05925478 · ClinicalTrials.gov registry record · Early Phase 1

Pterygopalatine Fossa Block in Aneurysmal Subarachnoid Hemorrhage

A Early Phase 1 study of Subarachnoid Hemorrhage, Aneurysmal, sponsored by University of Texas Southwestern Medical Center.

Completed
Registry status
Early Phase 1
Development phase
2
Enrollment target
1
Study location

NCT05925478 is a Early Phase 1 study of Subarachnoid Hemorrhage, Aneurysmal that has completed, run by University of Texas Southwestern Medical Center. The registered enrollment target is 2 participants, below the 163-participant average among 8 other Subarachnoid Hemorrhage, Aneurysmal trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05925478, a Early Phase 1 study of Subarachnoid Hemorrhage, Aneurysmal, has completed, sponsored by University of Texas Southwestern Medical Center.

COMPLETED
Registry status
Early Phase 1
Development phase
2 participants
Enrollment target
1
Study location

Study 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.

Interventions

  • PROCEDURE Ptergyopalatine Fossa Block
  • DRUG Bupivacaine 0.25% Injectable Solution

Study Locations (1)

Texas

  • UT Southwestern - Dallas

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2023-11-06
Est. Completion 2024-08-20
Phase Early Phase 1

What the Registry Record Tells You About NCT05925478

The ClinicalTrials.gov registry entry for NCT05925478 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 2 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 163-participant average among 8 other Subarachnoid Hemorrhage, Aneurysmal trials with a reported enrollment target (99% lower). The listed sponsor is University of Texas Southwestern Medical Center, which has 837 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Subarachnoid Hemorrhage, Aneurysmal appearing as the primary indexed condition, and to 2 interventions - of which Ptergyopalatine Fossa Block is the first listed.

NCT05925478 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT05925478 about?

NCT05925478 is a clinical study titled "Pterygopalatine Fossa Block in Aneurysmal Subarachnoid Hemorrhage". 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 de...

What is the current status of trial NCT05925478?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 2 participants. The study started on 2023-11-06. Estimated completion is 2024-08-20.

What conditions does trial NCT05925478 study?

This clinical trial studies the following conditions: Subarachnoid Hemorrhage, Aneurysmal.

What interventions are being tested in trial NCT05925478?

The interventions under investigation include: Ptergyopalatine Fossa Block (PROCEDURE), Bupivacaine 0.25% Injectable Solution (DRUG).

Who is sponsoring clinical trial NCT05925478?

This trial is sponsored by University of Texas Southwestern Medical Center, which has 837 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05925478 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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