Participants will receive one of the interventions (a daily dose of an oral steroid or placebo). Both groups will be asked to complete 6 surveys over 12 months and provide a daily pain score for up to 3 months.Ìý
You will not be able to participate in this study if you:
If you are interested, please contact us or complete your online pre-screen at:
Ìý
Ethics committee approval number:Ìý2019/740Ìý