Rilonacept (Arcalyst ®) in the Treatment of Subacromial Bursitis
Primary Purpose
Subacromial Bursitis
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Rilonacept
Corticosteroid
Sponsored by
About this trial
This is an interventional treatment trial for Subacromial Bursitis focused on measuring Rilonacept, Subacromial Bursitis treatment, Corticosteroid Injection
Eligibility Criteria
Inclusion Criteria:
- At least 18 years of age or older and at a minimum have a recent history (more than 3 days worth) of shoulder pain with moderate to severe tenderness to palpation over the subacromial bursa.
Exclusion Criteria:
- Allergies to lidocaine, marcaine, or kenalog.
- Allergies to rilonacept
- Flare of active inflammatory arthritis (such as a flare of Rheumatoid Arthritis)
- Gout or Pseudogout attack of the shoulder with subacromial tenderness
- Active infection
- Actively receiving chemotherapy, radiation therapy, or anticipating surgery for neoplasia
- Active myocardial infarction
- Clinical and/or radiographic evidence of a fracture (clavicular, humeral, or other).
Sites / Locations
- Keesler Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Rilonacept
Corticosteroid
Arm Description
160 mg of rilonacept will be injected in the subacromial bursa of participants in this arm.
80 mg (2 cc of 40 mg/mL) Kenalog intra-bursal once
Outcomes
Primary Outcome Measures
Improvement in Shoulder Function
The QuickDASH will be used as the primary outcome to assess improvement in pain and function of patients with clinical symptoms and signs of subacromial bursitis randomized to either rilonacept vs. corticosteroid injection. The QuickDASH is an 11 question form, a short version of the Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH). It ranges from 0 (no symptoms/full function) to 100 (maximal symptoms/no function). No units are specified. Cutoff scores: < 15 = no problem, 16 - 40 = problem, but working, > 40 = unable to work. US population mean +/- SD is 10.1 +/- 14.7.
Secondary Outcome Measures
Improvement in Pain
Secondary outcomes are improvement in pain (as assessed by patient self report, range between 0 and 10, with 0 as no pain and 10 described as the worst pain in their life).
Number of Participants With Adverse Events as a Measure of Safety and Tolerability
Any adverse event reported by the study participant during the four time points studied in the trial in either arm will be recorded.
Full Information
NCT ID
NCT01830699
First Posted
April 6, 2013
Last Updated
July 13, 2014
Sponsor
Keesler Air Force Base Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT01830699
Brief Title
Rilonacept (Arcalyst ®) in the Treatment of Subacromial Bursitis
Official Title
Rilonacept (Arcalyst ®) in the Treatment of Subacromial Bursitis
Study Type
Interventional
2. Study Status
Record Verification Date
July 2014
Overall Recruitment Status
Completed
Study Start Date
March 2013 (undefined)
Primary Completion Date
March 2014 (Actual)
Study Completion Date
March 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Keesler Air Force Base Medical Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To date no trials have been performed looking at whether or not intra-bursal injection of an IL-1 antagonist provides pain relief similar to that of a corticosteroid injection. The subcutaneous injection of anakinra, an IL-1 receptor antagonist, in patients with shoulder pain due to rotator cuff tendonitis and subacromial bursitis was efficacious in relieving pain but this information was presented as a case series in a letter to the editor format, so the validity of these results would require additional testing [Omoigui S, et al. 2004]. Based mainly on the data from the intra-articular administration of anakinra, there have not been any adverse trends in outcomes or safety to suggest that intra-bursal injection of rilonacept will carry an increase risk of adverse events. The purpose of this trial is to compare the improvement in pain and function of patients with clinical symptoms and signs of subacromial bursitis of rilonacept vs. corticosteroid injection (standard of care).
Detailed Description
Background: Subacromial bursitis is an inflammatory condition which is typically triggered by altered rotator cuff mechanics. One of the mainstays of therapy is corticosteroid injection. Given the inflammatory nature of subacromial bursitis coupled with prominence of interleukin-1 (IL-1) beta on histopathologic assessment of resected subacromial bursa, targeted anti-IL-1 therapy would be an attractive alternative to corticosteroid injection.
Hypothesis: One intra-bursal injection of the IL-1 trap rilonacept (Arcalyst ®), currently FDA approved for the treatment of cryopyrin associated periodic syndrome (CAPS), is non-inferior to intra-bursal corticosteroid injection at 4 weeks post-procedure.
Methods: This study is a prospective trial lasting a total of 4 weeks. Patients with typical symptoms and signs of subacromial bursitis are randomized to either corticosteroid injection prepared in the usual fashion in clinic vs. injection of rilonacept. Prior to injection of either medication patients will complete a QuickDASH Questionnaire and provide a verbal pain score from 0 to 10. The Quick DASH Questionnaire and verbal pain score are then completed within 2 duty days of injection, 2 weeks after injection, and 4 weeks after injection by phone.
Primary Outcome: Primary outcome is improvement in QuickDASH. Secondary outcomes are improvement in the verbal pain score and monitoring for infection or other complications from rilonacept administration.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Subacromial Bursitis
Keywords
Rilonacept, Subacromial Bursitis treatment, Corticosteroid Injection
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
33 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Rilonacept
Arm Type
Active Comparator
Arm Description
160 mg of rilonacept will be injected in the subacromial bursa of participants in this arm.
Arm Title
Corticosteroid
Arm Type
Placebo Comparator
Arm Description
80 mg (2 cc of 40 mg/mL) Kenalog intra-bursal once
Intervention Type
Drug
Intervention Name(s)
Rilonacept
Other Intervention Name(s)
Arcalyst
Intervention Description
160 mg intra-bursal once
Intervention Type
Drug
Intervention Name(s)
Corticosteroid
Other Intervention Name(s)
Triamcinolone (Kenalog)
Intervention Description
2 cc (40 mg/mL) triamcinolone intra-bursal once
Primary Outcome Measure Information:
Title
Improvement in Shoulder Function
Description
The QuickDASH will be used as the primary outcome to assess improvement in pain and function of patients with clinical symptoms and signs of subacromial bursitis randomized to either rilonacept vs. corticosteroid injection. The QuickDASH is an 11 question form, a short version of the Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH). It ranges from 0 (no symptoms/full function) to 100 (maximal symptoms/no function). No units are specified. Cutoff scores: < 15 = no problem, 16 - 40 = problem, but working, > 40 = unable to work. US population mean +/- SD is 10.1 +/- 14.7.
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Improvement in Pain
Description
Secondary outcomes are improvement in pain (as assessed by patient self report, range between 0 and 10, with 0 as no pain and 10 described as the worst pain in their life).
Time Frame
4 weeks
Title
Number of Participants With Adverse Events as a Measure of Safety and Tolerability
Description
Any adverse event reported by the study participant during the four time points studied in the trial in either arm will be recorded.
Time Frame
4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
At least 18 years of age or older and at a minimum have a recent history (more than 3 days worth) of shoulder pain with moderate to severe tenderness to palpation over the subacromial bursa.
Exclusion Criteria:
Allergies to lidocaine, marcaine, or kenalog.
Allergies to rilonacept
Flare of active inflammatory arthritis (such as a flare of Rheumatoid Arthritis)
Gout or Pseudogout attack of the shoulder with subacromial tenderness
Active infection
Actively receiving chemotherapy, radiation therapy, or anticipating surgery for neoplasia
Active myocardial infarction
Clinical and/or radiographic evidence of a fracture (clavicular, humeral, or other).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthew B Carroll, MD
Organizational Affiliation
Keesler Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Keesler Medical Center
City
Keesler AFB
State/Province
Mississippi
ZIP/Postal Code
39534
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
26184525
Citation
Carroll MB, Motley SA, Wohlford S, Ramsey BC. Rilonacept in the treatment of subacromial bursitis: A randomized, non-inferiority, unblinded study versus triamcinolone acetonide. Joint Bone Spine. 2015 Dec;82(6):446-50. doi: 10.1016/j.jbspin.2015.02.009. Epub 2015 Jul 13.
Results Reference
derived
Learn more about this trial
Rilonacept (Arcalyst ®) in the Treatment of Subacromial Bursitis
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