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Comparison of Two Methods of Transnasal Sphenopalatine Ganglion Block

NCT04479176 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 74

Last updated 2021-10-20

No results posted yet for this study

Summary

The transnasal sphenopalatine ganglion block(SPGB) is administered to patients with facial or head and neck pain. In the transnasal approach, the drip and topical methods are frequently used. We compared facial temperatures and VAS after transnasal SPGB.

Conditions

  • Sphenopalatine Ganglion Block

Interventions

PROCEDURE

Transnasal Sphenopalatine Ganglion Block

In transnasal approach, several authors described the traditional technique using sterile 10cm cotton tipped applicators that are dipped in the chosen anesthetic and then advanced along the superior border of the middle turbinate, until it reaches the posterior wall of the nasopharynx. Some other techniques had described dripping one or two ml of the anesthetics into the nostril.

Sponsors & Collaborators

  • Ajou University School of Medicine

    lead OTHER

Principal Investigators

  • Kim · Ajou University School of Medicine

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-10
Primary Completion
2021-10-01
Completion
2021-10-01

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04479176 on ClinicalTrials.gov