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SUSPENDED
NCT06023329
PHASE4

Superficial Cervical Plexus Block for Improved Outcomes in Pediatric Otolaryngologic Surgery

Sponsor: University of Minnesota

View on ClinicalTrials.gov

Summary

Literature on the use of superficial cervical plexus blocks for ear surgery is sparse in general, and almost non-existent in the pediatric population. Overall, literature review supports the safety of performance of this block but there is minimal published literature on its utility despite anecdotal evidence of benefit. This study, especially its prospective randomized nature will allow for expansion of the evidence for or against addition of this block to the care of pediatric patients undergoing ear surgery. The purpose of this study is to determine if SCPB plus standard practices provides superior pain control, as measured by reduced opiate consumption, compared to standard practices alone when performed on pediatric patients undergoing surgery on the ear and mastoid process.

Key Details

Gender

All

Age Range

3 Months - 18 Years

Study Type

INTERVENTIONAL

Enrollment

36

Start Date

2024-05-31

Completion Date

2027-05-01

Last Updated

2026-06-01

Healthy Volunteers

No

Interventions

DRUG

ropivacaine

will receive SCPB with ropivacaine via regional anesthesia team

DRUG

Saline

will receive SCPB with saline via regional anesthesia team

Locations (1)

University of Minnesota

Minneapolis, Minnesota, United States