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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.
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Inclusion and exclusion criteria
STUDY ELIGIBILITY CRITERIA:
Providing informed consent to participate in the study
18 to 64 years old
Any size closed wound from burn injury, occurring at least 3 weeks prior to enrollment in the study.
Use of regular medications for pain and/or itching control at stable doses for at least 3 weeks prior to enrollment in the study
No contraindications to tDCS:
Subject is not pregnant at the time of enrollment
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.
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Interventional model
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3 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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