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Peri-neural (N) for Rheumatoid Arthritis

N/A
Waitlist Available
Led By Nathan JD Brown, BMSc, MD
Research Sponsored by University of Calgary
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 72 hours
Awards & highlights

Study Summary

Brachial plexus nerve blocks provide superior analgesia over opioids while avoiding unwanted side effects. Single shot blocks with local anesthetic alone usually do not last the duration of the acute post-surgical pain period. This has led to the exploration of multiple adjuvants to increase the duration of single shot blocks, the most promising adjuvant being dexamethasone. Peri-neural administration is an off-label use of dexamethasone. While no adverse events have been reported in human clinical studies, logic would dictate that we minimize the dose needed to produce the desired effect. Most studies thus far have used peri-neural dexamethasone doses ranging from 4-10 mg. However, Albrecht et al. found no difference in block duration comparing 4 mg and 8 mg doses while Liu et al. reported equivalent block duration using doses of 1, 2 and 4 mg. Recent studies have evaluated whether systemic and peri-neural administrations of dexamethasone are equivalent, which would in turn imply a site of action. Results have been mixed. Four studies concluded peri-neural and intravenous administration are equivalent at prolonging analgesia, though one study had methodological errors, including the administration of intravenous dexamethasone to all patients. All of these studies used dexamethasone doses of 8 to 10 mg. One study where a lower dose (4 mg) was used found that peri-neural administration prolonged block duration whereas intravenous did not. With that, the rationale of our study is to determine if equivalent block-prolonging analgesia can be achieved using low dose (1 mg) dexamethasone given peri-neural or intravenous. Clinical experience at our centre has been that 1 mg dexamethasone added to 20 mL produces similar block duration to that reported in published studies using higher doses.

Eligible Conditions
  • Rheumatoid Arthritis
  • Osteoarthritis
  • Nerve Compression
  • Ligament Injury

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~72 hours
This trial's timeline: 3 weeks for screening, Varies for treatment, and 72 hours for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Time to first sensation of pain at the surgical site.
Secondary outcome measures
duration of motor blockade
incidence of nausea and vomiting and pruritus in the first 48 h
morphine or morphine equivalent usage in the first 48 h postoperatively
+2 more

Trial Design

3Treatment groups
Experimental Treatment
Placebo Group
Group I: Peri-neural (N)Experimental Treatment1 Intervention
Peri-neural Dexamethasone 1 mg
Group II: IntravenousExperimental Treatment1 Intervention
Intravenous Dexamethasone 1 mg
Group III: Control (C)Placebo Group1 Intervention
Control intervention (no dexamethasone)

Find a Location

Who is running the clinical trial?

University of CalgaryLead Sponsor
792 Previous Clinical Trials
868,848 Total Patients Enrolled
1 Trials studying Rheumatoid Arthritis
528 Patients Enrolled for Rheumatoid Arthritis
Nathan JD Brown, BMSc, MDPrincipal InvestigatorUniversity of Calgary

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~35 spots leftby May 2025