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Effects of Transcranial Direct Current Stimulation (tDCS) on Neuropathic Symptoms Due to Burn Injury

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Mass General Brigham

Status

Completed

Conditions

Pain
Burn Injury

Treatments

Device: Transcranial Direct Current Stimulation (tDCS)

Study type

Interventional

Funder types

Other

Identifiers

NCT01404026
2010-p-001209

Details and patient eligibility

About

The purpose of this study is to investigate the effects of transcranial direct current stimulation (tDCS) on the neuropathic symptoms (pain/itch) due to a burn injury. The investigators hypothesize that the active tDCS group will show a significant pain/itch reduction when compared to sham stimulation.

Enrollment

3 patients

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

STUDY ELIGIBILITY CRITERIA:

  1. Providing informed consent to participate in the study

  2. 18 to 64 years old

  3. Any size closed wound from burn injury, occurring at least 3 weeks prior to enrollment in the study.

    • Subjects with burns in scalp area will be excluded from the study as the electrode may cause irritation to the injuries
  4. Use of regular medications for pain and/or itching control at stable doses for at least 3 weeks prior to enrollment in the study

  5. No contraindications to tDCS:

    • metallic implants in the head
    • implanted brain medical devices
  6. Subject is not pregnant at the time of enrollment

  7. Neuropathic pain or itching (rated at least 4 on the VAS) within the burn scar or donor site, (pain can be described as burning, stabbing, piercing, pins and needles, tearing sensation) for at least 3 weeks.

Please note: If a patient reports pain and itching, we will enroll the patient based upon their most dominant symptom.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

3 participants in 2 patient groups

Active tDCS
Active Comparator group
Description:
Subjects will undergo 20 minutes of active tDCS stimulation.
Treatment:
Device: Transcranial Direct Current Stimulation (tDCS)
Sham tDCS
Sham Comparator group
Description:
Subjects will undergo sham tDCS stimulation, where the current is only active for 30 seconds.
Treatment:
Device: Transcranial Direct Current Stimulation (tDCS)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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