N/A
Completed N=24
Pilot Study of Transcranial Stimulation (tDCS)to Relieve Neuropathic Pain in Cancer Patients
Source: ClinicalTrials.gov NCT01948050 ↗Enrolled (actual)
24
Serious AEs
8.3%
Results posted
Jul 2014
Primary outcomePrimary: Pain Intensity — 1.66; 1.60 Points on numerical rating scale
Summary
This is a pilot study designed to collect preliminary data on safety and efficacy of transcranial direct current stimulation (tDCS) to relieve pain in cancer patients who developed neuropathic pain in the affected area after a surgical intervention, radiation therapy, or chemotherapy to treat the disease.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pain Intensity |
1.66; 1.60 | — |
Eligibility Criteria
Adult male and female patients with cancer who developed neuropathic pain in the affected area secondary the surgical procedure, chemotherapy or radiation that meet the following Inclusion/Exclusion criteria:
Inclusion Criteria
Pain on the side of the lesion
- Spontaneous pain with a score for "worst pain in the last 24 hours" >4 on a numeric scale 0-10
- Must present the following symptoms and signs:
- Continuous burning, shooting, or lancinating pain.
- Presence of hyperesthesia
- Presence of hyperalgesia (to pinprick) and/or allodynia (to light touch)
Exclusion Criteria
- Uncontrolled hypertension, uncontrolled diabetes, uncontrolled cardiovascular disease
- Pain/painful conditions unrelated to the cancer or related treatment
- Pregnancy
- History of seizures/epilepsy
- Any implanted devices (e.g. a cardio stimulator, etc)
- Active illegal drug/alcohol abuse
- Unable to follow directions or complete tools in English
Data sourced from ClinicalTrials.gov (NCT01948050). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.