A Trial Comparing Glenohumeral Joint Steroid Injection Versus Suprascapular Nerve Block in Patients With Frozen Shoulder (TIFFS)
Primary Purpose
Frozen Shoulder
Status
Recruiting
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Glenohumeral joint steroid injection
Suprascapular nerve block steroid injection
Sponsored by
About this trial
This is an interventional treatment trial for Frozen Shoulder
Eligibility Criteria
Inclusion Criteria:
- Patient diagnosed with unilateral frozen shoulder, age greater than or equal to 18 years. Diagnosis of frozen shoulder will be based on clinical examination (restriction of passive external rotation in the affected shoulder > 50% compared to opposite site), in the presence of normal plain radiographs (antero-posterior and axillary projections) (other than calcific tendinopathy).
Exclusion Criteria:
- Age less than 18 years, lacking capacity/unable to give valid consent for participation, full thickness rotator cuff tear diagnosed on either Ultrasound scan or Magnetic Resonance Imaging, unable to complete follow up, unable to speak or read English, allergy to corticosteroid or local anaesthetic, simultaneous bilateral frozen shoulder.
Sites / Locations
- Blackpool Victoria Hospitals NHS Foundation TrustRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Glenohumeral joint injection
Suprascapular nerve block
Arm Description
Ultrasound guided steroid injection into the glenohumeral joint (10mls of 1% lidocaine with 40mg depo-medrone)
Ultrasound guided steroid injection as a suprascapular nerve block at the spinoglenoid notch adjacent to the nerve as it traverses under the spinoglenoid ligament (10mls of 1% lidocaine with 40mg depo-medrone)
Outcomes
Primary Outcome Measures
Oxford Shoulder Score (OSS) (Scored 12-60, higher score means worse outcome)
Patient will complete in clinic
Secondary Outcome Measures
Oxford Shoulder Score (Scored 12-60, higher score means worse outcome)
Patient will complete over telephone/by post
Pain Numeric Rating Scale (Scored 0-10, higher score means worse outcome)
Patient will complete over telephone/by post
Quick Disabilities of Arm, Shoulder and Hand (QuickDASH) (Scored 0-100, higher score means worse outcome)
Patient will complete over telephone/by post
EuroQol-5 Dimension-5 level (EQ-5D-5L)(, First part does not have min or max values and not scored on numerical scale. EQ VAS part is scored 0-100, high score means better outcome)
Patient will complete over telephone/by post
Full Information
NCT ID
NCT04965376
First Posted
July 7, 2021
Last Updated
September 11, 2023
Sponsor
Blackpool Teaching Hospitals NHS Foundation Trust
1. Study Identification
Unique Protocol Identification Number
NCT04965376
Brief Title
A Trial Comparing Glenohumeral Joint Steroid Injection Versus Suprascapular Nerve Block in Patients With Frozen Shoulder
Acronym
TIFFS
Official Title
Therapeutic Injections for Frozen Shoulder (TIFFS Study)- Comparing Suprascapular Nerve Block Versus Intra-articular Glenohumeral Joint Injection. A Randomised Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2021 (Actual)
Primary Completion Date
August 2024 (Anticipated)
Study Completion Date
August 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Blackpool Teaching Hospitals NHS Foundation Trust
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this study is to determine if there is any difference in terms of pain relief in patients with frozen shoulder, when given a steroid injection as a suprascapular nerve block compared to a glenohumeral joint intra-articular injection.
The investigators hypothesis is that there is a significant difference in terms of pain relief at 3 months, 6 months and 1 year between a steroid injection as a suprascapular nerve block compared to a glenohumeral joint intra-articular injection.
Participants who attend the orthopaedic clinic and are diagnosed with unilateral frozen shoulder and who are suitable to be treated with a steroid injection will be identified. If the participant consents to having a steroid injection, he/she will then be invited to participate in the trial where they will have an injection either into the glenohumeral joint (ball and socket joint of the shoulder) or as a suprascapular nerve block (injection adjacent to a nerve over the shoulder blade) under ultrasound guidance. Participants will then be followed up at 3, 6 and 12 months after their injection and asked to complete a set of questionnaires assessing pain, function and movement. The results of the groups will then be compared to see if one treatment is superior to the other.
Detailed Description
This is a single centre, parallel, two-arm, randomized clinical trial. The trial is expected to take a total of 3 years with 12-18 months for patient recruitment, 12 months for follow up and 6-12 months for data collection, analysis and publication.
The null hypothesis is that there will be no differences in terms of pain relief at 3 months, 6 months and 1 year between a steroid injection as a suprascapular nerve block compared to a glenohumeral joint intra-articular injection.
Adult patients diagnosed with unilateral frozen shoulder who are suitable to be treated with a steroid injection will receive a verbal explanation of the study by a suitably qualified member of the research team alongside an information leaflet. Eligible, consented participants will be randomised in a 1:1 ratio by the selection of sealed, opaque envelopes with one of the two injection types documented inside. Participants will be free to withdraw from the study at any time without prejudice. The injection types include an ultrasound guided steroid injection into the glenohumeral joint (10mls of 1% lidocaine with 40mg depo-medrone) or an ultrasound guided steroid injection as a suprascapular nerve block at the spinoglenoid notch adjacent to the nerve as it traverses under the spinoglenoid ligament (10mls of 1% lidocaine with 40mg depo-medrone. Following both injections, participants are taken through a protocol of physiotherapy for their frozen shoulder over the subsequent 3 months. Participants will be seen back in the outpatient clinic 3 months after their injection to review their progress and collect follow-up data. Further follow-up data will be collected by the completion of questionnaires via post at 6 months and 12 months after the injection. The primary outcome measure of this study is the Oxford Shoulder Score (OSS) at 3 months post-injection. Secondary end points include Oxford Shoulder Score at 6 months and 1 year, pain using the Pain Numeric Rating Scale at 3 months, 6 months and 1 year, Quick Disabilities of Arm, Shoulder and Hand (QuickDASH) questionnaire at 3 months, 6 months and 1 year and EQ-5D-5L at 3 months, 6 months and 1 year.
Baseline demographic and clinical variables will be reported using summary statistics. In terms of the primary outcome, the change in total Oxford Shoulder Score from baseline to 3 months post-injection will be compared between the two groups using either the Independent Samples t-Test or Mann-Whitney U Test, with the final choice depending on an exploration of the data. The same approach will be adopted for secondary outcomes. All analysis will be performed according to the intention to treat principle.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Frozen Shoulder
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Ultrasound guided steroid injection into the glenohumeral joint versus ultrasound guided suprascapular nerve block
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Glenohumeral joint injection
Arm Type
Active Comparator
Arm Description
Ultrasound guided steroid injection into the glenohumeral joint (10mls of 1% lidocaine with 40mg depo-medrone)
Arm Title
Suprascapular nerve block
Arm Type
Active Comparator
Arm Description
Ultrasound guided steroid injection as a suprascapular nerve block at the spinoglenoid notch adjacent to the nerve as it traverses under the spinoglenoid ligament (10mls of 1% lidocaine with 40mg depo-medrone)
Intervention Type
Procedure
Intervention Name(s)
Glenohumeral joint steroid injection
Intervention Description
Ultrasound guided steroid injection into the glenohumeral joint (10mls of 1% lidocaine with 40mg depo-medrone)
Intervention Type
Procedure
Intervention Name(s)
Suprascapular nerve block steroid injection
Intervention Description
Ultrasound guided steroid injection as a suprascapular nerve block at the spinoglenoid notch adjacent to the nerve as it traverses under the spinoglenoid ligament (10mls of 1% lidocaine with 40mg depo-medrone)
Primary Outcome Measure Information:
Title
Oxford Shoulder Score (OSS) (Scored 12-60, higher score means worse outcome)
Description
Patient will complete in clinic
Time Frame
3 months post-injection
Secondary Outcome Measure Information:
Title
Oxford Shoulder Score (Scored 12-60, higher score means worse outcome)
Description
Patient will complete over telephone/by post
Time Frame
6 months and 12 months post-injection
Title
Pain Numeric Rating Scale (Scored 0-10, higher score means worse outcome)
Description
Patient will complete over telephone/by post
Time Frame
3 months, 6 months and 12 months post-injection
Title
Quick Disabilities of Arm, Shoulder and Hand (QuickDASH) (Scored 0-100, higher score means worse outcome)
Description
Patient will complete over telephone/by post
Time Frame
3 months, 6 months and 12 months post-injection
Title
EuroQol-5 Dimension-5 level (EQ-5D-5L)(, First part does not have min or max values and not scored on numerical scale. EQ VAS part is scored 0-100, high score means better outcome)
Description
Patient will complete over telephone/by post
Time Frame
3 months, 6 months and 12 months post-injection
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age greater than or equal to 18 years
Patient diagnosed with unilateral frozen shoulder (Diagnosis of frozen shoulder will be based on clinical examination (restriction of passive external rotation in the affected shoulder > 50% compared to opposite site), in the presence of normal plain radiographs (antero-posterior and axillary projections) (other than calcific tendinopathy))
Exclusion Criteria:
Age less than 18 years
Lacking capacity/unable to give valid consent for participation
Full thickness rotator cuff tear diagnosed on either Ultrasound scan or Magnetic Resonance Imaging
Unable to complete follow up
Unable to speak or read English
Allergy to corticosteroid or local anaesthetic
Simultaneous bilateral frozen shoulder.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Charalambos P Charalambous
Phone
01253 300000
Email
mr.charalambous@nhs.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charalambos P Charalambous
Organizational Affiliation
Blackpool Teaching Hospitals NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Blackpool Victoria Hospitals NHS Foundation Trust
City
Blackpool
State/Province
Lancashire
ZIP/Postal Code
FY3 8NR
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Charalambos P Charalambous
Phone
01253 300000
Email
mr.charalambous@nhs.net
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Data will be published in peer review journal on completion of the study.
Learn more about this trial
A Trial Comparing Glenohumeral Joint Steroid Injection Versus Suprascapular Nerve Block in Patients With Frozen Shoulder
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