ClinicalTrials.Veeva

Menu

Comparison of Pain-Related Changes in Cerebral Blood Volume in Burn Patients With Neuropathic Pain

H

Hangang Sacred Heart Hospital

Status

Unknown

Conditions

Neuropathic Pain

Treatments

Diagnostic Test: magnetic resonance imaging(MRI)

Study type

Observational

Funder types

Other

Identifiers

NCT04125576
HangangSHH-5

Details and patient eligibility

About

The investigators will observe increased or decreased CBV in patients with thermal injury compared with the CBV in healthy controls.

Full description

Prevalence of chronic pain has been shown to be high after thermal injury. Post-burn neuropathic pain causes chronic disabilities that is often difficult to treat effectively.

To study changes in the pain network associated with neuropathic pain, magnetic resonance imaging(MRI) will be used to evaluate cerebral blood volume(CBV) in patients who was injuried by burn. Over the fifty participants will be recruited. The participants will be comprised 30 subjects with neuropathic pain caused by thermal injury and 20 healthy contols. The 30 patients with neuropathic pain will be comprised divided into 15 electrical injury group and 15 non-electrical burn injury group. The patients are included the patients with severe neuropathic pain that is rated at least 5 on the visual analogue scale (VAS), despite treatments with gabapentin medication and other physical modalities. The intensity of neuropathic pain will be measured using the visual analogue scale(VAS). Depressive mood will be assessed using the Beck Depression Scale. CBV maps will be compared between burn patients and controls. And the relationship between individual participant CBV(measured in voxels), BDS and VAS score will be also examined.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Burn patients
  • severe neuropatic pain rated at least 5 on the 10-point numerical rating scale (NRS).

Exclusion criteria

  • cardiac arrest history
  • history of neurologic disease or brain surgery
  • unstable heart disease or presence of a cardiac pacemaker
  • psychiatric disorder
  • diabetes mellitus
  • abnormal renal function
  • contraindication for MRI
  • pregnancy.

Trial design

50 participants in 2 patient groups

Burn patients
Description:
The subjects complaine of severe neuropathic pain that is rated at least 5 on the visual analogue scale (VAS), despite treatments with gabapentin medication and other physical modalities.
Treatment:
Diagnostic Test: magnetic resonance imaging(MRI)
Healthy controls
Description:
age and sex matched healthy controls
Treatment:
Diagnostic Test: magnetic resonance imaging(MRI)

Trial contacts and locations

1

Loading...

Central trial contact

Cheong Hoon Seo, Dr.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems