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Pain and Perceptual Distortion of Face

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University of Aarhus

Status

Completed

Conditions

Orofacial Pain
Neuropathic Pain

Treatments

Device: Active repetitive transcranial magnetic stimulation (rTMS)
Device: Sham repetitive transcranial magnetic stimulation (sham rTMS)

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Post-traumatic trigeminal neuropathic pain (PTNP) is "a unilateral or bilateral facial or oral pain following and caused by trauma to the trigeminal nerve(s), with other symptoms and/or clinical signs of trigeminal nerve dysfunction, and persisting or recurring for more than 3 months". PTNP may result from a major craniofacial/oral trauma or may be subsequent to relatively minor dental treatments such as teeth extractions, surgeries, root canal treatment. Patients suffering from this condition have a significantly reduced quality of life. Unfortunately, the currently available management modalities are associated with limited success and side effects.

Repetitive transcranial magnetic stimulation (rTMS), which is a safe, non-invasive brain stimulation technique has emerged as a potential treatment for chronic pain. In this study, the purpose is to explore the potential of rTMS in treating the persistent neuropathic pain by providing individualized treatment for the sufferers.

Full description

In addition to pain, a curious observation in people with PTNP is that they report that the painful facial area is "swollen" or "feels differently". There are often no clinical signs or physical differences present, hence such self-reported "illusions" may represent a kind of disrupted body image or a "perceptual distortion" of the face and can be speculated to contribute to the maintenance of facial pain. rTMS paradigms are being widely applied in both therapeutic and investigative studies.In this project, the aim is to employ continuous theta-burst stimulation (cTBS), an inhibitory rTMS paradigm, to evaluate its effect on pain perception and PD in people with PTNP.

In this project, people with PTNP (N=9) received a rTMS (50 Hz, 600 pulses for 40s) session/week as intervention for four consecutive weeks at the primary somatosensory cortex (face area) in a "n-of-1" single-blinded randomized controlled cross-over design: (A) active-sham-active-sham or (B) sham-active-sham-active. That is the same participant received both active and sham either in the (A) order or (B). Pain intensity and perceptual distortion (PD) as perceived size changes of the affected face area were measured at baseline, immediately, 60 mins after rTMS in each session and end of the session (a week after rTMS), one and three months after rTMS. Questionnaires on quality of life, jaw function, sleep quality were also assessed. Changes in pain and PD after each intervention were evaluated.

Enrollment

12 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Persistent Post-traumatic trigeminal neuropathic pain patients for 6 months or longer
  • Stable on analgesic medication

Exclusion criteria

  • past history of TMS therapy or TMS-related contraindications (pacemaker, epilepsy etc.).
  • Major stroke
  • Pregnancy
  • Severe organic brain damage

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

12 participants in 2 patient groups

Active group
Active Comparator group
Description:
Continuous theta burst stimulation
Treatment:
Device: Active repetitive transcranial magnetic stimulation (rTMS)
Sham group
Sham Comparator group
Description:
Sham repetitive transcranial magnetic stimulation (rTMS)
Treatment:
Device: Sham repetitive transcranial magnetic stimulation (sham rTMS)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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