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Anti-TNF (adalimumab) injection for the treatment of adults with frozen shoulder during the pain predominant stage protocol for a multi-centre, randomised, double blind, parallel group, feasibility trial.
- Source :
-
NIHR open research [NIHR Open Res] 2023 Apr 24; Vol. 2, pp. 28. Date of Electronic Publication: 2023 Apr 24 (Print Publication: 2022). - Publication Year :
- 2023
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Abstract
- Objectives: The Anti-Freaze-F trial will assess the feasibility of conducting a large randomised controlled trial to assess whether intra-articular injection of anti-TNF (adalimumab) can reduce pain and improve function in people with pain predominant early stage frozen shoulder.<br />Methods and Analysis: We are conducting a multi-centre, randomised feasibility study, with an embedded qualitative sub-study. We will recruit adults ≥18 years with a new episode of shoulder pain attributable to early stage frozen shoulder, recruited from at least five UK NHS musculoskeletal and related physiotherapy services. Participants (n=84) will be randomised (centralised computer generated 1:1 allocation) to receive either: 1) intra-articular injection of anti-TNF (adalimumab 160mg) or 2) placebo injection (saline [0.9% sodium chloride]), both under ultrasound guidance. A second injection of the allocated treatment (adalimumab 80mg) or equivalent volume of placebo will be administered 2-3 weeks later. All participants will receive a physiotherapy advice leaflet providing education and advice about frozen shoulder and pain management. The primary feasibility objectives are: 1) the ability to screen and identify potential participants with pain predominant early stage frozen shoulder; 2) willingness of eligible participants to consent and be randomised to intervention; 3) practicalities of delivering the intervention, including time to first injection and number of participants receiving second injection; 4) standard deviation of the Shoulder Pain and Disability Index (SPADI) score and attrition rate at 3 months (i.e. 12 weeks) post-randomisation in order to estimate the sample size for a definitive trial. We will also assess follow up rates and viability of patient-reported outcome measures and range of shoulder motion for a definitive trial. Research Ethics Committee approval (REC 21/NE/0214).<br />Trial Registration Number: ISRCTN 27075727; EudraCT number: 2021-003509-23; ClinicalTrials.gov NCT05299242.<br />Competing Interests: Competing interests: Professor Sir Marc Feldman and Professor Jagdeep Nanchahal are co-founders and hold equity in 180 Life Sciences, the company funding the purchase of adalimumab, the investigational medicinal product to be used in this trial.<br /> (Copyright: © 2023 Hopewell S et al.)
Details
- Language :
- English
- ISSN :
- 2633-4402
- Volume :
- 2
- Database :
- MEDLINE
- Journal :
- NIHR open research
- Publication Type :
- Academic Journal
- Accession number :
- 37881307
- Full Text :
- https://doi.org/10.3310/nihropenres.13275.2