ClinicalTrials.Veeva

Menu

Mechanisms and Treatment of Post-amputation Neuropathic Pain

University of Oslo (UIO) logo

University of Oslo (UIO)

Status

Terminated

Conditions

Neuropathic Pain
Amputation
Phantom Limb Pain

Treatments

Drug: Spinal anaesthesia (sub-study 1)
Device: Repetitive transcranial magnetic stimulation (sub-study 2)

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Phantom and residual limb pain are types of peripheral neuropathic pain that are difficult to treat and where the underlying mechanisms are still not fully understood. Repetitive transcranial magnetic stimulation (rTMS) of the motor cortex is an increasingly studied technique for the treatment of neuropathic pain and has shown modest effects in pain intensity reduction for the treatment of neuropathic pain. Newer rTMS coils provide the opportunity to stimulate larger brain areas, which could provide a better treatment option compared to conventional coils. The aims of this study are to investigate whether the peripheral nervous system is a necessary driver of phantom limb pain and/or residual limb pain in patients with lower limb amputation using spinal anaesthesia, and to assess the analgesic efficacy of deep H-coil rTMS compared to sham stimulation in the same patients.

Enrollment

1 patient

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-80 years of age
  • Unilateral or bilateral lower limb amputation resulting in residual limb pain and/or phantom pain, fulfilling the criteria for definite neuropathic pain
  • Usual pain intensity at least 4/10 over the past 24 hrs using the numerical scale of the BPI at screening
  • Daily pain
  • Pain for at least 3 months
  • Stable pharmacological treatment for pain or no pharmaceutical treatment at least 1 month prior to the study
  • Patients who can be followed for the whole duration of the study
  • Minimum 4/10 pain intensity at the time of spinal anaesthesia for sub-study 1

Exclusion criteria

  • Any clinically significant or unstable medical or psychiatric disorder
  • Subjects protected by law (guardianship or tutelage measure)
  • History of or current substance abuse (alcohol, drugs)
  • Pending litigation
  • Contraindications to spinal anaesthetic block (e.g. use of prescribed or non-prescribed medication that can increase risk of bleeding such as anticoagulants, non-steroidal anti-inflammatory drugs and acetylsalicylic acid)
  • Contraindication to rTMS (past severe head trauma, history of epilepsy or ongoing epilepsy, active cerebral tumour, past neurosurgical intervention, intracranial hypertension, implanted devices not compatible such as cardiac pacemaker and neurostimulator, cochlear implants, pregnancy or lactation. All women of childbearing age will be required to have negative pregnancy test at inclusion and to be using contraception)
  • Other pain conditions more severe than phantom and residual limb pain.
  • Inability to understand the protocol or to fill out the forms
  • Other ongoing research protocol or recent past protocol within one month before the inclusion

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

1 participants in 2 patient groups

Active and then sham repetitive transcranial magnetic stimulation
Other group
Description:
Deep rTMS is delivered with the Brainsway H7-coil (Brainsway, Jerusalem, Israel) applied via a helmet placed on the head targeting the primary motor cortex of the leg. Sham stimulation is delivered with a sham coil placed in the helmet encasing the active rTMS coil. Sham rTMS sessions will use exactly the same parameters of stimulation as active rTMS.
Treatment:
Drug: Spinal anaesthesia (sub-study 1)
Device: Repetitive transcranial magnetic stimulation (sub-study 2)
Sham and then active repetitive transcranial magnetic stimulation
Other group
Description:
Deep rTMS is delivered with the Brainsway H7-coil (Brainsway, Jerusalem, Israel) applied via a helmet placed on the head targeting the primary motor cortex of the leg.Sham stimulation is delivered with a sham coil placed in the helmet encasing the active rTMS coil. Sham rTMS sessions will use exactly the same parameters of stimulation as active rTMS.
Treatment:
Drug: Spinal anaesthesia (sub-study 1)
Device: Repetitive transcranial magnetic stimulation (sub-study 2)

Trial contacts and locations

1

Loading...

Central trial contact

Per Hansson, PhD; Nadine Farnes, MSc

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems