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TENS for Phantom Limb Pain Prevention Following Major Amputation

Transcutaneous Electrical Nerve Stimulation (TENS) for Phantom Limb Pain Prevention Following Arteriopathic Major Amputation: Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02496351
Enrollment
40
Registered
2015-07-14
Start date
2015-05-31
Completion date
2017-03-31
Last updated
2015-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peripheral Vascular Diseases, Phantom Limb Pain

Keywords

transcutaneous electrical nerve stimulation

Brief summary

A growing body of literature indicates that up to 80% of amputees may have phantom limb pain (PLP). The first cause for limb loss is vascular disease. Usually, amputees who suffer from PLP are suboptimal treated. Therefore, many amputees are disabled by their chronic pain. The etiology and pathophysiology of PLP are poorly understood. Some studies suggest a somatosensory cortex reorganization. Transcutaneous Electrical Nerve Stimulation (TENS) is a analgesic technique. TENS apply a low voltage electrical current through the skin using surface electrodes in order to stimulate afferent nerve fibbers. Because of the lack of evidence to support any treatment for PLP, interest has turned to preventing it instead. The aim of this study is to assess if the early use of TENS in the immediately postoperative of major limb amputation due to peripheral vascular disease, should decrease the PLP incidence. TENS should interfere in the mechanism of PLP production to level of the pain fibers conduction.

Detailed description

Introduction: Postamputation pain is highly prevalent after vascular limb amputation. The physiopathological basis should be divided in supraspinal, spinal and peripheral mechanisms. Supraspinal mechanism involve somatosensory cortical reorganization; spinal reorganization in the dorsal horn, occurs after deafferentation from peripheral nerve injury and peripherical nerve injury begins with the nerve section in surgery. All this factors seems to end into a somatosensory cortex reorganization. In this sense, it seems that our ability to prevent PLP depend on the capability to modulate the plasticity of the Central Nervous System (CNS). Transcutaneous electrical nerve stimulation it´s a safe, easy and inexpensive analgesic technique acting on the conduction pathways of pain. An adequated program is mandatory: balanced symmetrical biphasic pulse, pulse length greater than 250microsg, modulated high frequency and electrodes placed over the dermatomes corresponding to lumbar-sacral spine; will be used in the intervention patients Hypothesis: In patients with TENS use during the immediately postoperative of major limb amputation due to peripheral vascular disease, phantom limb pain will appear with less frequency than in control patients. Study population: Patients undergoing major limb amputation for peripheral vascular disease. Study design: A randomized, prospective, blinded (patient, physician, statistician),clinical trial placebo versus intervention group study has been design. In the intervention arm, TENS should be applied during the 24 hours immediately after limb amputation. The placebo arm, also will carry TENS but without an active program. All patients should receive the standard analgesic treatment for limb amputation during their hospitalization time. Evaluation and objectives: Before surgery all patients made two test for pain evaluation: The Analogical Visual Scale and the DN4 questionnaire for neuropathic pain. At 3 days, 1 month and 3 months after surgery, all patients will be evaluated about their pain using the recommended test for neuropathic pain:The Analogical Visual Scale and the DN4 (neuropathic pain 4) questionnaire for neuropathic pain . Also, at month 1 and 3th, two more test should be done in order to evaluate quality of life: The SF-12 (short form-12) health survey questionnaire about health and the Medical Outcomes Study (MOS) for sleep test.

Interventions

DEVICETENS INTERVENTION

24 hours of TENS treatment in the immediately postoperative of limb amputation

Sponsors

Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age over 18 years of both genders * Critical limb ischemia (arteriopathic or diabetic aetiology) * MINI MENTAL TEST (minimum 24 points)

Exclusion criteria

* Pace marker * Don´t speak Spanish * Not agreement with the study * Dermatological lesion affecting the electrode place

Design outcomes

Primary

MeasureTime frameDescription
PREOPERATIVE PAIN EVALUATION3 days before interventionAnalogical Visual Scale: the patient indicate its pain level in the scale witch has an interval between 0-10 DN4 Test ( for neurophatic pain). This is the recommended test of the Spanish association on Anesthesiology for determinate neurophatic pain.
PREOPERATIVE NEUROPAThIC PAIN EVALUATION3 days before interventionDN4 Test ( for neuropathic pain). This is the recommended test of the Spanish association on Anesthesiology for determinate neuropathic pain. It consist in several questions to evaluate the clinical situation and some others about the physical situation.

Secondary

MeasureTime frameDescription
1 MONTH POSTOPERATIVE HEALTH EVALUATION1 MONTHTest SF-12 about health situation. This is the recommended test of the Spanish Pain society for subjective evaluation of health situations. It consist in 12 questions about its own perceptions, employment status, daily activities, frame of mind
1 MONTH POSTOPERATIVE SLEEP EVALUATION1 MONTHTest MOS (Sleep Scale from the Medical Outcomes Study) Some questions for sleep evaluation
INMEDIATELY POSTOPERATIVE PAIN EVALUATION3 days after interventionAnalogical Visual Scale: the patient indicate its pain level in the scale witch has an interval between 0-10
3 MONTH POSTOPERATIVE HEALTH EVALUATION3 MONTHTest SF-12 about health situation. This is the recommended test of the Spanish Pain society for subjective evaluation of health situations. It consist in 12 questions about its own perceptions, employment status, daily activities, frame of mind
3 MONTH POSTOPERATIVE SLEEP EVALUATION3 MONTHTest MOS (Sleep Scale from the Medical Outcomes Study) Some questions for sleep evaluation
3 MONTH POSTOPERATIVE PAIN EVALUATION3 MONTHAnalogical Visual Scale: the patient indicate its pain level in the scale witch has an interval between 0-10
1 MONTH POSTOPERATIVE PAIN EVALUATION1 MONTHAnalogical Visual Scale: the patient indicate its pain level in the scale witch has an interval between 0-10

Countries

Spain

Contacts

Primary ContactBarbara Bodega, Mrs
barcabo@icloud.com+34696962685
Backup ContactVanesa Rodenas, Mrs
rodena_van@gva.es+34961925963

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026