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01.12.2018 | Study protocol | Ausgabe 1/2018 Open Access

BMC Musculoskeletal Disorders 1/2018

Routine versus on demand removal of the syndesmotic screw; a protocol for an international randomised controlled trial (RODEO-trial)

BMC Musculoskeletal Disorders > Ausgabe 1/2018
S. A. Dingemans, M. F. N. Birnie, F. R. K. Sanders, M. P. J. van den Bekerom, M. Backes, E. van Beeck, F. W. Bloemers, B. van Dijkman, E. Flikweert, D. Haverkamp, H. R. Holtslag, J. M. Hoogendoorn, P. Joosse, M. Parkkinen, G. Roukema, N. Sosef, B. A. Twigt, R. N. van Veen, A. H. van der Veen, J. Vermeulen, J. Winkelhagen, B. C. van der Zwaard, S. van Dieren, J. C. Goslings, T. Schepers



Syndesmotic injuries are common and their incidence is rising. In case of surgical fixation of the syndesmosis a metal syndesmotic screw is used most often. It is however unclear whether this screw needs to be removed routinely after the syndesmosis has healed. Traditionally the screw is removed after six to 12 weeks as it is thought to hamper ankle functional and to be a source of pain. Some studies however suggest this is only the case in a minority of patients. We therefore aim to investigate the effect of retaining the syndesmotic screw on functional outcome.


This is a pragmatic international multicentre randomised controlled trial in patients with an acute syndesmotic injury for which a metallic syndesmotic screw was placed. Patients will be randomised to either routine removal of the syndesmotic screw or removal on demand. Primary outcome is functional recovery at 12 months measured with the Olerud-Molander Score. Secondary outcomes are quality of life, pain and costs. In total 194 patients will be needed to demonstrate non-inferiority between the two interventions at 80% power and a significance level of 0.025 including 15% loss to follow-up.


If removal on demand of the syndesmotic screw is non-inferior to routine removal in terms of functional outcome, this will offer a strong argument to adopt this as standard practice of care. This means that patients will not have to undergo a secondary procedure, leading to less complications and subsequent lower costs.

Trial registration

This study was registered at the Netherlands Trial Register (NTR5965), (NCT02896998) on July 15th 2016.
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