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TerminatedNCT04831255Updated May 13, 2025

ZILRETTA™ for Treatment of Idiopathic Adhesive Capsulitis

A Phase 1 interventional study of triamcinolone acetonide extended-release injectable suspension in Adhesive Capsulitis, Frozen Shoulder and Adhesive Capsulitis of Shoulder, sponsored by University of Virginia. Terminated at 1 site in United States. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2025-05-13.

Sponsored by University of Virginia · Phase 1, Interventional, and Treatment

Why this study was terminated
Not able to find enough subjects

From the registry’s dates

  • Primary completion was Aug 2023, 3 years 1 month ago, and no results have been posted to the registry.
  • Registered 1 year 9 months after the study started (first participant enrolled Jun 2019, registered Mar 2021).
Phase
Phase 1
Study type
Interventional
Enrollment
39
Allocation
Not applicable
Ages
18 Years to 80 Years
Sex
All
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Study 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.

Read the 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.

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Conditions studied

  • Adhesive Capsulitis
  • Frozen Shoulder
  • Adhesive Capsulitis of Shoulder

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03

In context

Bursitis

411 studies on the registry are indexed under Bursitis; 113 are open to participants now.

This study's enrollment of 39 is below the median of 45 across 371 interventional studies indexed under Bursitis.

Browse Bursitis studies →

Lead sponsor

University of Virginia is the lead sponsor of 653 studies on the registry; 134 are open to participants now.

Of its 60 completed or terminated interventional studies of FDA-regulated products, 41 (68%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
39 participants (actual)

Study arms

  • Experimental
    ZILRETTA

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

    Drug: triamcinolone acetonide extended-release injectable suspension

Interventions

  • Drugtriamcinolone acetonide extended-release injectable suspension

    ZILRETTA (triamcinolone acetonide extended-release injectable suspension) injection in the glenohumeral joint administered under ultrasound guidance.

    Also known as: ZILRETTA

06

What researchers measure

Primary outcomes

  1. Visual Analog Scale Score

    Pain rating on a scale of 0-10, higher numbers indicating a worse outcome

    Time frame: 6 months after injection

Secondary outcomes

  1. 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.

    Time frame: 6 months after injection

  2. 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.

    Time frame: 12 months after injection

  3. 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.

    Time frame: 6 months after injection

  4. 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.

    Time frame: 12 months after injection

  5. Triplanar Range of Motion

    Shoulder range of motion

    Time frame: 1 month after injection

  6. Triplanar Range of Motion

    Shoulder range of motion

    Time frame: 3 months after injection

  7. Triplanar Range of Motion

    Shoulder range of motion

    Time frame: 6 months after injection

  8. Triplanar Range of Motion

    Shoulder range of motion

    Time frame: 12 months after injection

  9. Need for another injection

    Yes or no answer if the patient needed another corticosteroid injection during their time enrolled in the study

    Time frame: 12 months after injection

  10. Time to second injection (if applicable)

    how long after the ZILRETTA injection the patient needed another corticosteroid injection

    Time frame: 12 months after injection

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Study locations

1 site
  • University of Virginia
    Charlottesville, Virginia 22908, United States
08

References and documents

Study documents

  • Informed consent form · Jun 21, 2019

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 13, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04831255
Lead sponsor
University of Virginia
Responsible party
Brian Werner, MD (Assistant Professor, Department of Orthopaedic Surgery, University of Virginia) — Principal investigator
First posted
Apr 5, 2021
Start date
Jun 21, 2019
Primary completion
Aug 31, 2023
Completion
Aug 31, 2023
Last update
May 13, 2025

Study contacts

Brian Werner, MD
principal investigator · University of Virginia

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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