The SAInT study: a protocol for a randomized controlled trial of steroid injection for subacromial pain syndrome using the anterolateral versus posterior approach

Author:

Charalambous Charalambos P.12ORCID,Hirst John T.1,Kwaees Tariq3,Lane Suzanne1,Taylor Clare1,Solanki Nilesh1,Maley Alex4,Taylor Rebecca4ORCID,Howell Laura4,Nyangoma Stephen4,Martin Francis L.4ORCID,Khan Maqsood1,Choudhry Muhammad N.1,Shetty Vishwanath1,Malik Rayaz A.5ORCID

Affiliation:

1. Department of Trauma and Orthopaedics, Blackpool Victoria Hospital, Blackpool, UK

2. School of Medicine, University of Central Lancashire, Preston, UK

3. St Helens and Knowsley Teaching Hospitals NHS Foundation Trust, Prescot, UK

4. Department of Research and Development, Clinical Research Centre, Blackpool Victoria Hospital, Blackpool, UK

5. Department of Medicine, Weill Cornell Medicine-Qatar, Doha, Qatar

Abstract

AimsSteroid injections are used for subacromial pain syndrome and can be administered via the anterolateral or posterior approach to the subacromial space. It is not currently known which approach is superior in terms of improving clinical symptoms and function. This is the protocol for a randomized controlled trial (RCT) to compare the clinical effectiveness of a steroid injection given via the anterolateral or the posterior approach to the subacromial space.MethodsThe Subacromial Approach Injection Trial (SAInT) study is a single-centre, parallel, two-arm RCT. Participants will be allocated on a 1:1 basis to a subacromial steroid injection via either the anterolateral or the posterior approach to the subacromial space. Participants in both trial arms will then receive physiotherapy as standard of care for subacromial pain syndrome. The primary analysis will compare the change in Oxford Shoulder Score (OSS) at three months after injection. Secondary outcomes include the change in OSS at six and 12 months, as well as the Pain Numeric Rating Scale (0 = no pain, 10 = worst pain), Disabilities of Arm, Shoulder and Hand questionnaire (DASH), and 36-Item Short-Form Health Survey (SF-36) (RAND) at three months, six months, and one year after injection. Assessment of pain experienced during the injection will also be determined. A minimum of 86 patients will be recruited to obtain an 80% power to detect a minimally important difference of six points on the OSS change between the groups at three months after injection.ConclusionThe results of this trial will demonstrate if there is a difference in shoulder pain and function after a subacromial space steroid injection between the anterolateral versus posterior approach in patients with subacromial pain syndrome. This will help to guide treatment for patients with subacromial pain syndrome.Cite this article: Bone Jt Open 2024;5(9):729–735.

Publisher

British Editorial Society of Bone & Joint Surgery

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