TY - JOUR
T1 - Prevention of postamputation pain with targeted muscle reinnervation (PreventPAP trial)
T2 - protocol for a national, multicentre, randomised, sham-controlled trial
AU - Tendijck, Guus A.H.
AU - van Schaik, Jan
AU - Dijkman, Robert R.
AU - Niesters, Marieke
AU - van Zwet, Erik W.
AU - van den Hout, Wilbert B.
AU - Ploeg, Arianne J.
AU - van Rijt, Willem G.
AU - de Ruiter, Godard C.W.
AU - Coert, J. Henk
AU - Duraku, Liron S.
AU - Zuidam, J. Michiel
AU - van de Water, Willemien
AU - Pondaag, Willem
AU - van der Krogt, Hanneke
AU - Groen, Justus L.
AU - Verduijn, Pieter S.
AU - Overgoor, Max L.E.
AU - Malessy, Martijn J.A.
AU - Mees, Barend M.E.
AU - Rijken, Bianca
AU - van Wijk, Marieke P.
AU - Kwee, Esmee
AU - Brakkee, Elise M.
AU - de Jong, Tim
AU - van der Steenhoven, Tim J.
AU - Jongkind, Vincent
AU - Yeung, Kak Khee
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2025.
PY - 2025/11/4
Y1 - 2025/11/4
N2 - Introduction In the Netherlands, approximately 2200 major amputations of the lower extremities are performed each year, the majority in vascular patients. Around 61% of these patients will develop postamputation pain (PAP). PAP is a severe, lifelong, disabling condition profoundly affecting quality of life. During amputations, the common practice is to cut the nerves without employing nerve-surgical techniques to prevent chronic pain due to neuroma formation. In recent years, targeted muscle reinnervation (TMR) has been the most frequently studied technique for treating PAP, inhibiting neuroma formation by rerouting the cut mixed nerve to a functional motor nerve. We hypothesise that a primary TMR procedure during major lower limb amputations will result in a lower prevalence of PAP. Methods and analysis We propose a national, multicentre, randomised, sham-controlled trial comparing TMR with traction neurectomy in major amputations of the lower extremities in patients with vascular disease. 203 patients will be recruited with an indication for a transfemoral to transtibial amputation as a primary or secondary sequela of vascular disease. The subjects are randomly assigned to the TMR group or the traction neurectomy group. PAP will be evaluated 1 year postoperatively as the primary endpoint. Secondary outcomes include quality of life, mobility, neuropathic pain, hospital anxiety and depression, cost-effectiveness and complications. Ethics and dissemination This study has been reviewed and approved by the local ethical review body, ‘The Medical Ethics Committee Leiden The Hague Delft’, under the reference: P24.073 on 28 November 2024. Results will be published in peer-reviewed journals. Trial registration number NCT06719245. Dutch trial registry: NL87196.058.24
AB - Introduction In the Netherlands, approximately 2200 major amputations of the lower extremities are performed each year, the majority in vascular patients. Around 61% of these patients will develop postamputation pain (PAP). PAP is a severe, lifelong, disabling condition profoundly affecting quality of life. During amputations, the common practice is to cut the nerves without employing nerve-surgical techniques to prevent chronic pain due to neuroma formation. In recent years, targeted muscle reinnervation (TMR) has been the most frequently studied technique for treating PAP, inhibiting neuroma formation by rerouting the cut mixed nerve to a functional motor nerve. We hypothesise that a primary TMR procedure during major lower limb amputations will result in a lower prevalence of PAP. Methods and analysis We propose a national, multicentre, randomised, sham-controlled trial comparing TMR with traction neurectomy in major amputations of the lower extremities in patients with vascular disease. 203 patients will be recruited with an indication for a transfemoral to transtibial amputation as a primary or secondary sequela of vascular disease. The subjects are randomly assigned to the TMR group or the traction neurectomy group. PAP will be evaluated 1 year postoperatively as the primary endpoint. Secondary outcomes include quality of life, mobility, neuropathic pain, hospital anxiety and depression, cost-effectiveness and complications. Ethics and dissemination This study has been reviewed and approved by the local ethical review body, ‘The Medical Ethics Committee Leiden The Hague Delft’, under the reference: P24.073 on 28 November 2024. Results will be published in peer-reviewed journals. Trial registration number NCT06719245. Dutch trial registry: NL87196.058.24
UR - https://www.scopus.com/pages/publications/105021348280
U2 - 10.1136/bmjopen-2025-105053
DO - 10.1136/bmjopen-2025-105053
M3 - Article
AN - SCOPUS:105021348280
SN - 2044-6055
VL - 15
JO - BMJ Open
JF - BMJ Open
IS - 11
M1 - e105053
ER -