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Clinical Trials/NCT03657173
NCT03657173
Completed
Not Applicable

Ultrasound Image Quality of the Brachial Plexus at the Interscalene Space Before and After Shoulder Arthroscopy: a Prospective Cohort Study

Mayo Clinic1 site in 1 country30 target enrollmentJune 18, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Postoperative
Sponsor
Mayo Clinic
Enrollment
30
Locations
1
Primary Endpoint
Change in Likert Scale
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Ultrasound guided interscalene nerve blockade with local anesthesia is a standard regional anesthetic technique for providing postoperative analgesia during shoulder arthroscopy and wide variety of shoulder procedures. There is a paucity of data regarding the effects of shoulder arthroscopy on ultrasound image quality, including the effects of muscle mobilization and the use of large volume irrigation and subsequent tissue absorption, though increased neck circumference and airway edema are known complications of arthroscopic shoulder procedures.

The objective of the study is to determine if there is a difference in ultrasound image quality of the interscalene block anatomy, by Likert scale, pre- versus post-operatively in a cohort of patients undergoing shoulder arthroscopy who routinely receive blockade of the brachial plexus for postoperative analgesia. Further, if there are differences in imaging quality, correlations with surgical and patient factors will be studied.

Registry
clinicaltrials.gov
Start Date
June 18, 2018
End Date
November 30, 2018
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Bridget P. Pulos

Principal Investigator

Mayo Clinic

Eligibility Criteria

Inclusion Criteria

  • Subject is undergoing shoulder procedures involving arthroscopy
  • Subject has consented to interscalene blockade for postoperative analgesia

Exclusion Criteria

  • Patient refusal
  • Contraindications to interscalene blockade, including significant pulmonary insufficiency, hemi-diaphragmatic paralysis, brachial plexus or degenerative neuropathy
  • Allergy to proposed local anesthetic medication\\
  • Severe cervical spine disease.
  • BMI \>40 kg/m2
  • Neck Circumference \> 50cm
  • Failed preoperative interscalene blockade
  • Patients known to be currently pregnant or actively breastfeeding
  • Patients where English is a language barrier

Outcomes

Primary Outcomes

Change in Likert Scale

Time Frame: 2-3 months

Ultrasound media will be scored using a Likert scale (from 1-5 based on quality of imaging) individually for pre-operative and post-operative scanning for each enrolled patient

Study Sites (1)

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