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Intra-articular Doxycycline: A Novel Treatment of Adhesive Capsulitis (DOXY)

Primary Purpose

Adhesive Capsulitis, Adhesive Capsulitis of Unspecified Shoulder, Frozen Shoulder

Status
Terminated
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Methylprednisolone Injectable Product
Doxycycline Injection
Sponsored by
Vanderbilt University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adhesive Capsulitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 18 years of age and older,
  • diagnosis of stage II adhesive capsulitis as determined by clinical examination of the treating physician, and
  • absence of abnormal findings on X-ray.

Exclusion Criteria:

  • allergy to Doxycycline or Methylprednisolone,
  • pregnancy,
  • diagnosis,
  • Inflammatory arthritis or diabetes,
  • secondary adhesive capsulitis (history of significant trauma, rotator cuff tear injury, stroke)
  • evidence of arthritis on x-ray,
  • current infectious disease, and
  • any previous treatment for the for adhesive capsulitis of the affected shoulder.

Sites / Locations

  • Vanderbilt Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Methylprednisolone

Doxycycline

Arm Description

Patients meeting the inclusion criteria will be randomized into either the control group of intra-articular injection of 40mg Methylprednisolone once every 2 two weeks for 4 weeks (day 1, week 2, week 4) with 20 patients in each group. Injections will be administered by the treating physician.

Patients meeting the inclusion criteria will be randomized or the experimental group of intraarticular injection of 50 mg doxycycline once every 2 two weeks for 4 weeks (day 1, week 2, week 4), with 20 patients in each group. Injections will be administered by the treating physician.

Outcomes

Primary Outcome Measures

Change in American Shoulder and Elbow Score (ASES)
The American Shoulder and Elbow Score questionnaire was developed to provide a standardized method for evaluating shoulder function and has been validated in patients with any array of shoulder pathologies. ASES results are in the 0 to 100 range, where 0 indicates a worse shoulder condition and 100 indicates best shoulder condition, so the lower the score, the greater the level of shoulder disability. Transforming the pain and the ADLs domains into the final score relies on the following formulas: Pain = 5 x (10 - Score from question 7)
Change in Range of Motion(ROM) Measurements
The ROM measurements will include forward flexion, abduction, external rotation at the side and at 90 degrees abduction, and internal rotation at the side and at 90 degrees abduction recorded by the treating physician at follow up visits

Secondary Outcome Measures

Number of Medical Co-morbidities
number of medical co-morbidities per participant
Duration of Symptoms
Length of time participants have experienced shoulder symptoms
Changes in Pain
Number of participants with current dominant symptom and/or dominant symptom with disease onset
Pain With Sitting
Number of patients that have pain while sitting or have ever had pain while sitting will be recorded using patient-reported survey and review of the patient's electronic medical record in Epic.
Stiffness
Number of participants with current dominant symptom and/or dominant symptom with disease onset

Full Information

First Posted
March 20, 2018
Last Updated
April 21, 2023
Sponsor
Vanderbilt University Medical Center
Collaborators
Orthopedic Research and Education Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT03479502
Brief Title
Intra-articular Doxycycline: A Novel Treatment of Adhesive Capsulitis
Acronym
DOXY
Official Title
Intra-articular Doxycycline: A Novel Treatment of Adhesive Capsulitis
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Terminated
Why Stopped
Lack of personnel to help with recruiting
Study Start Date
January 5, 2018 (Actual)
Primary Completion Date
February 8, 2022 (Actual)
Study Completion Date
February 8, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University Medical Center
Collaborators
Orthopedic Research and Education Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
We will recruit a total of 40 patients from the Vanderbilt Sports Medicine Clinics who have been diagnosed with adhesive capsulitis and have not undergone any previous treatment. The 40 patients will be randomized, with 20 in the control group of 3 intra-articular injections of 40mg Methylprednisolone spaced every two weeks, and 20 in the experimental group of 3 intra-articular injection of 50mg doxycycline spaced every two weeks. Both groups will begin a standardized physical therapy program within a pain-free range of motion 4 weeks after the initiation of treatment. We will prospectively follow patients for one year, with follow-up at 6 weeks, 12 weeks, 6 months, and 12 months after the initiation of treatment. Outcomes will be measured using the American Shoulder and Elbow Score (ASES) and objective measurements of shoulder range of motion, which will be collected by the treating physician. Both the patients and physicians participating in the study will be blinded.
Detailed Description
Adhesive capsulitis, also known as frozen shoulder, is a common condition of the shoulder joint affecting 2-5% of the adult population and characterized by progressive, painful loss of both passive and active range of motion of shoulder [1,2]. Individuals affected by this condition find it increasingly difficult to perform activities of daily living that require overhead movement or rotation of the affected shoulder. The natural history of frozen shoulder follows a predictable progression of symptoms, lasting from 9-24 months before complete resolution, and results in significant loss of productivity and quality of life for those affected [3]. Despite the significant number of patients affected by adhesive capsulitis and the extensive literature focused on the progression and natural history of the condition, the true underlying etiology remains poorly understood. In light of this poor understanding of the condition, it is not surprising that a number of conservative and invasive modalities exist as accepted treatments. These include non-steroidal anti-inflammatory drugs (NSAIDS), oral steroids, intra-articular steroid injections, Physical Therapy (PT), and benign neglect as well as more invasive treatments such as hydroxylation, manipulation under anesthesia, and arthroscopic capsular release [2]. These treatments have all be shown to have short-term benefit in pain relief, but none have proven to be superior nor alter the long-term natural history of adhesive capsulitis. Over the past decade, however, there has been a growing body of literature suggesting that Propionibacterium acnes infection may play a significant role in a variety of pathological conditions affecting the native shoulder, most notably frozen shoulder [4,5]. Our goal is to employ a treatment strategy focused on eradicating P acnes infection as a conservative treatment of adhesive capsulitis. Through this project, we aim to complete a prospective randomized pilot study to examine the hypothesis that administration of intra-articular antibiotics effective against P acnes will prove to be a superior treatment of adhesive capsulitis as compared to current gold standard of intraarticular steroid injection.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Patients meeting the inclusion criteria will be randomized into either the control group of intra-articular injection of 40mg Methylprednisolone once every 2 two weeks for 4 weeks (day 1, week 2, week 4) or the experimental group of intraarticular injection of 50 mg doxycycline once every 2 two weeks for 4 weeks (day 1, week 2, week 4), with 20 patients in each group. Injections will be administered by the treating physician. The Vanderbilt Investigational Pharmacy will provide the doxycycline and the steroid solutions and will be in charge of patient randomization.
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Double Blind Masking
Allocation
Randomized
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Methylprednisolone
Arm Type
Active Comparator
Arm Description
Patients meeting the inclusion criteria will be randomized into either the control group of intra-articular injection of 40mg Methylprednisolone once every 2 two weeks for 4 weeks (day 1, week 2, week 4) with 20 patients in each group. Injections will be administered by the treating physician.
Arm Title
Doxycycline
Arm Type
Active Comparator
Arm Description
Patients meeting the inclusion criteria will be randomized or the experimental group of intraarticular injection of 50 mg doxycycline once every 2 two weeks for 4 weeks (day 1, week 2, week 4), with 20 patients in each group. Injections will be administered by the treating physician.
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone Injectable Product
Other Intervention Name(s)
Prednisone
Intervention Description
3 intra-articular injections of Methylprednisolone Injectable Product spaced every two weeks
Intervention Type
Drug
Intervention Name(s)
Doxycycline Injection
Other Intervention Name(s)
Doxy
Intervention Description
3 intra-articular injections of Doxycycline Injection spaced every two weeks
Primary Outcome Measure Information:
Title
Change in American Shoulder and Elbow Score (ASES)
Description
The American Shoulder and Elbow Score questionnaire was developed to provide a standardized method for evaluating shoulder function and has been validated in patients with any array of shoulder pathologies. ASES results are in the 0 to 100 range, where 0 indicates a worse shoulder condition and 100 indicates best shoulder condition, so the lower the score, the greater the level of shoulder disability. Transforming the pain and the ADLs domains into the final score relies on the following formulas: Pain = 5 x (10 - Score from question 7)
Time Frame
Baseline and 12 months
Title
Change in Range of Motion(ROM) Measurements
Description
The ROM measurements will include forward flexion, abduction, external rotation at the side and at 90 degrees abduction, and internal rotation at the side and at 90 degrees abduction recorded by the treating physician at follow up visits
Time Frame
Baseline and 12 months
Secondary Outcome Measure Information:
Title
Number of Medical Co-morbidities
Description
number of medical co-morbidities per participant
Time Frame
Baseline
Title
Duration of Symptoms
Description
Length of time participants have experienced shoulder symptoms
Time Frame
Baseline
Title
Changes in Pain
Description
Number of participants with current dominant symptom and/or dominant symptom with disease onset
Time Frame
Baseline
Title
Pain With Sitting
Description
Number of patients that have pain while sitting or have ever had pain while sitting will be recorded using patient-reported survey and review of the patient's electronic medical record in Epic.
Time Frame
Baseline
Title
Stiffness
Description
Number of participants with current dominant symptom and/or dominant symptom with disease onset
Time Frame
Baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18 years of age and older, diagnosis of stage II adhesive capsulitis as determined by clinical examination of the treating physician, and absence of abnormal findings on X-ray. Exclusion Criteria: allergy to Doxycycline or Methylprednisolone, pregnancy, diagnosis, Inflammatory arthritis or diabetes, secondary adhesive capsulitis (history of significant trauma, rotator cuff tear injury, stroke) evidence of arthritis on x-ray, current infectious disease, and any previous treatment for the for adhesive capsulitis of the affected shoulder.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John E Kuhn, MD
Organizational Affiliation
Study Director
Official's Role
Study Director
Facility Information:
Facility Name
Vanderbilt Medical Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
21167743
Citation
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Results Reference
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Citation
Neviaser AS, Hannafin JA. Adhesive capsulitis: a review of current treatment. Am J Sports Med. 2010 Nov;38(11):2346-56. doi: 10.1177/0363546509348048. Epub 2010 Jan 28.
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Citation
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Citation
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Citation
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Citation
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Intra-articular Doxycycline: A Novel Treatment of Adhesive Capsulitis

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