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ZILRETTA™ for Treatment of Idiopathic Adhesive Capsulitis

Primary Purpose

Adhesive Capsulitis, Frozen Shoulder, Adhesive Capsulitis of Shoulder

Status
Recruiting
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
triamcinolone acetonide extended-release injectable suspension
Sponsored by
University of Virginia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adhesive Capsulitis

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of idiopathic adhesive capsulitis (onset <6 months prior)
  • Pain rating of 5 or greater out of 10 on 0-10 scale at time of enrollment
  • Willing to come on site for follow up evaluations at 1 month, 3 months, 6 months, and 12 months after the injection

Exclusion Criteria:

  • Active workers compensation case
  • Known psychiatric disorders under active treatment
  • Uncontrolled diabetes (defined as diabetic ketoacidosis, severe peripheral neuropathy, ophthalmologic or renal manifestations)
  • Diagnosed osteoarthritis of the ipsilateral or contralateral shoulder
  • Painful joint condition in another part of the body affecting perceived pain

Sites / Locations

  • University of VirginiaRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

ZILRETTA

Arm Description

Single injection of triamcinolone acetonide extended-release injectable suspension, injected in the glenohumeral joint under ultrasound guidance.

Outcomes

Primary Outcome Measures

Visual Analog Scale Score
Pain rating on a scale of 0-10, higher numbers indicating a worse outcome

Secondary Outcome Measures

American Shoulder and Elbow Society Score
Pain and function patient reported outcome for the shoulder. Scores range from 0 to 100 with a score of 0 indicating a worse shoulder condition and 100 indicating a better shoulder condition.
American Shoulder and Elbow Society Score
Pain and function patient reported outcome for the shoulder. Scores range from 0 to 100 with a score of 0 indicating a worse shoulder condition and 100 indicating a better shoulder condition.
PROMIS Physical Function Score
Patient reported outcome measuring physical function level measured by T scores and standard deviations. The average is 50, so a T score lower than 50 indicates a worse outcome.
PROMIS Physical Function Score
Patient reported outcome measuring physical function level measured by T scores and standard deviations. The average is 50, so a T score lower than 50 indicates a worse outcome.
Triplanar Range of Motion
Shoulder range of motion
Triplanar Range of Motion
Shoulder range of motion
Triplanar Range of Motion
Shoulder range of motion
Triplanar Range of Motion
Shoulder range of motion
Need for another injection
Yes or no answer if the patient needed another corticosteroid injection during their time enrolled in the study
Time to second injection (if applicable)
how long after the ZILRETTA injection the patient needed another corticosteroid injection

Full Information

First Posted
March 31, 2021
Last Updated
April 5, 2021
Sponsor
University of Virginia
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1. Study Identification

Unique Protocol Identification Number
NCT04831255
Brief Title
ZILRETTA™ for Treatment of Idiopathic Adhesive Capsulitis
Official Title
A Stratified Investigation of a Single Injection of ZILRETTA™ (Triamcinolone Acetonide Extended-release Injectable Suspension) for Symptomatic Relief in Patients With Idiopathic Adhesive Capsulitis of the Shoulder
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Recruiting
Study Start Date
June 21, 2019 (Actual)
Primary Completion Date
July 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Adhesive capsulitis is a fairly common orthopedic condition that causes pain and loss of range of motion. There are a variety of ways to treat adhesive capsulitis, one of them being an intra-articular steroid injection. This is done to help decrease the inflammatory response caused by adhesive capsulitis. In this study, all participants will receive an intra-articular glenohumeral injection of ZILRETTA and will be followed up with at four time points over 1 year to observe pain, function and range of motion following the injection.
Detailed Description
Adhesive capsulitis is a painful shoulder condition characterized by a gradual loss of both passive and active range of motion due to inflammatory changes and eventual fibrosis and contracture of the shoulder joint capsule. It occurs in about 2% to 5% of the population, and a majority of patients are female. The true cause of the condition remains unclear, however, it has been proposed that the initial synovitis stimulates the development of a fibrotic cascade. The development of adhesive capsulitis has been associated with diabetes mellitus, thyroid dysfunction, Dupuytrens contractures, autoimmune diseases and treatments for certain cancers. Adhesive capsulitis progresses through four predictable phases, defined by symptoms, physical examination, arthroscopic appearance and biopsies. Regardless of stage, the mainstay of treatment for adhesive capsulitis of the shoulder is conservative, focused mainly on physical therapy combined with a home exercise program, regardless of stage. Pharmacologic agents are often used as adjuncts to physical therapy, and include nonsteroidal anti-inflammatory medications (NSAIDs), oral corticosteroids and intra-articular injections of corticosteroids. Although a large percentage of patients in the early stages of disease respond well to conservative treatments, those who fail therapy and injections may require surgical intervention, including arthroscopy with lysis of adhesions and/or manipulation under anesthesia. Numerous studies have investigated the effect and success of injections combined with standard physical therapy for adhesive capsulitis of the shoulder. In general, intra-articular injection of corticosteroids has been found to be superior to administration of oral cortisone and at least equivalent to manipulation under anesthesia alone. Injections have been shown to reduce pain quicker and result in earlier return of range of motion. Low doses of steroid appear equally as effective as higher doses. Image-guided injections, whether ultrasound or fluoroscopic guided injections, have also been shown to be more effective than blinded injections. Failure of an injection and therapy to provide relief either results in a repeat image-guided injection or surgical intervention, both of which have significant associated cost and potential morbidity. Thus, there would be significant potential value to a long-acting, sustained release intra-articular steroid injection for the treatment of adhesive capsulitis of the shoulder. Zilretta®, triamcinolone acetonide extended release suspension 32 mg, is a microsphere formulation of injectable steroid which is FDA-approved for and has shown significant promise for the treatment of knee osteoarthritis. This long-acting steroid could have several important advantages in the treatment of shoulder adhesive capsulitis. It may potentiate and prolong the anti-inflammatory effect of the steroid, and potentially avoid the need for costly additional image-guided injections or expensive and potentially morbid surgery. An additional potential benefit is less elevation of peripheral blood glucose in diabetics, a known complication of traditional steroid injections that has been demonstrated to be mitigated using a sustained release formulation. Out primary aim in this study is to assess patient reported pain and outcomes in patients with idiopathic adhesive capsulitis of the shoulder at 3, 6 and 12 months following single, image guided ZILRETTA injection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adhesive Capsulitis, Frozen Shoulder, Adhesive Capsulitis of Shoulder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Model Description
All subjects receive the ZILRETTA injection
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ZILRETTA
Arm Type
Experimental
Arm Description
Single injection of triamcinolone acetonide extended-release injectable suspension, injected in the glenohumeral joint under ultrasound guidance.
Intervention Type
Drug
Intervention Name(s)
triamcinolone acetonide extended-release injectable suspension
Other Intervention Name(s)
ZILRETTA
Intervention Description
ZILRETTA (triamcinolone acetonide extended-release injectable suspension) injection in the glenohumeral joint administered under ultrasound guidance.
Primary Outcome Measure Information:
Title
Visual Analog Scale Score
Description
Pain rating on a scale of 0-10, higher numbers indicating a worse outcome
Time Frame
6 months after injection
Secondary Outcome Measure Information:
Title
American Shoulder and Elbow Society Score
Description
Pain and function patient reported outcome for the shoulder. Scores range from 0 to 100 with a score of 0 indicating a worse shoulder condition and 100 indicating a better shoulder condition.
Time Frame
6 months after injection
Title
American Shoulder and Elbow Society Score
Description
Pain and function patient reported outcome for the shoulder. Scores range from 0 to 100 with a score of 0 indicating a worse shoulder condition and 100 indicating a better shoulder condition.
Time Frame
12 months after injection
Title
PROMIS Physical Function Score
Description
Patient reported outcome measuring physical function level measured by T scores and standard deviations. The average is 50, so a T score lower than 50 indicates a worse outcome.
Time Frame
6 months after injection
Title
PROMIS Physical Function Score
Description
Patient reported outcome measuring physical function level measured by T scores and standard deviations. The average is 50, so a T score lower than 50 indicates a worse outcome.
Time Frame
12 months after injection
Title
Triplanar Range of Motion
Description
Shoulder range of motion
Time Frame
1 month after injection
Title
Triplanar Range of Motion
Description
Shoulder range of motion
Time Frame
3 months after injection
Title
Triplanar Range of Motion
Description
Shoulder range of motion
Time Frame
6 months after injection
Title
Triplanar Range of Motion
Description
Shoulder range of motion
Time Frame
12 months after injection
Title
Need for another injection
Description
Yes or no answer if the patient needed another corticosteroid injection during their time enrolled in the study
Time Frame
12 months after injection
Title
Time to second injection (if applicable)
Description
how long after the ZILRETTA injection the patient needed another corticosteroid injection
Time Frame
12 months after injection

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of idiopathic adhesive capsulitis (onset <6 months prior) Pain rating of 5 or greater out of 10 on 0-10 scale at time of enrollment Willing to come on site for follow up evaluations at 1 month, 3 months, 6 months, and 12 months after the injection Exclusion Criteria: Active workers compensation case Known psychiatric disorders under active treatment Uncontrolled diabetes (defined as diabetic ketoacidosis, severe peripheral neuropathy, ophthalmologic or renal manifestations) Diagnosed osteoarthritis of the ipsilateral or contralateral shoulder Painful joint condition in another part of the body affecting perceived pain
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kaitlyn Shank, MEd, ATC
Phone
434-243-5653
Email
kshank@virginia.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Lizzie Leitch, MEd, ATC
Phone
434-243-0256
Email
ebl7nu@hscmail.mcc.virginia.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brian Werner, MD
Organizational Affiliation
University of Virginia
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Virginia
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kaitlyn Shank, MEd, ATC
Phone
434-243-5653
Email
kshank@virginia.edu
First Name & Middle Initial & Last Name & Degree
Lizzie Leitch, MEd, ATC
Phone
434-243-0256
Email
ebl7nu@hscmail.mcc.virginia.edu
First Name & Middle Initial & Last Name & Degree
Brian Werner, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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ZILRETTA™ for Treatment of Idiopathic Adhesive Capsulitis

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