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Local Anesthetic

Nerve Block for Spinal Cord Injury-Related Shoulder Pain

Phase 4
Waitlist Available
Led By Timothy Tiu, MD
Research Sponsored by University of Miami
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 12 months
Awards & highlights

Study Summary

This trial will test if a suprascapular nerve block can help people with chronic shoulder pain and spinal cord injury.

Eligible Conditions
  • Chronic Shoulder Pain

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Number of participants at each Global Satisfaction Rating (GSR)
Number of participants reporting treatment related adverse events
Secondary outcome measures
Change in BPI-I scores
Change in DASH Questionnaire scores
Change in NRS scores
+1 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: Suprascapular Nerve Block in Participants with Spinal Cord Injuries (SCI) GroupExperimental Treatment3 Interventions
Participants in this group will receive standard of care (SOC) suprascapular nerve block using a mixture of Lidocaine and Triamcinolone.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Suprascapular Nerve Block
2022
N/A
~90
Lidocaine
FDA approved
Triamcinolone
FDA approved

Find a Location

Who is running the clinical trial?

University of MiamiLead Sponsor
898 Previous Clinical Trials
409,651 Total Patients Enrolled
Timothy Tiu, MDPrincipal InvestigatorUniversity of Miami

Media Library

Lidocaine 1% Injectable Solution (Local Anesthetic) Clinical Trial Eligibility Overview. Trial Name: NCT05364099 — Phase 4
Chronic Shoulder Pain Research Study Groups: Suprascapular Nerve Block in Participants with Spinal Cord Injuries (SCI) Group
Chronic Shoulder Pain Clinical Trial 2023: Lidocaine 1% Injectable Solution Highlights & Side Effects. Trial Name: NCT05364099 — Phase 4
Lidocaine 1% Injectable Solution (Local Anesthetic) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05364099 — Phase 4

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are individuals aged 30 or more eligible to participate in this research?

"The age range that this trial is willing to accept patients is between 18 to 70 years old."

Answered by AI

Has the FDA cleared Suprascapular Nerve Block for public use?

"Suprascapular Nerve Block is a Phase 4 trial, meaning that it is an approved treatment, and thus it received a score of 3."

Answered by AI

What benefits does this clinical trial hope to bring patients?

"The primary metric for success in this clinical trial is the number of patients that experience adverse events related to the treatment, which will be measured a month after the procedure. Additionally, the study will look at secondary objectives like changes in DASH Questionnaire scores (a measure of ability to perform upper extremity activities), number of participants at each Global Satisfaction Rating, and changes in NRS scores (a measure of pain levels)."

Answered by AI

Are there still vacancies in this research project for test subjects?

"According to the latest update on clinicaltrials.gov, this particular study is not looking for new patients at this time. The trial was initially posted on 1/1/2023, with the most recent edit on 7/30/2022. There are 448 other trials that are open for recruitment."

Answered by AI
~0 spots leftby Apr 2025