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- Klinische proef NCT02863315
The Effects of Anodal tsDCS on Chronic Neuropathic Pain After SCI
The Effects of Anodal Transcutaneous Spinal Direct Current Stimulation on Chronic Neuropathic Pain After Spinal Cord Injury: Pilot Study
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Studietype
Inschrijving (Verwacht)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
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Seoul, Korea, republiek van, 03080
- Seoul National University
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- cervical or upper thoracic complete motor spinal cord injury, at least 6 months after SCI, 20<=age<90
- neuropathic pain (LANSS score >= 12), stable chronic pain for at least the three preceding months but not over 5 years
- score higher than or equal to 4 cm (0 cm = 'no pain' and 10 cm = 'worst possible pain') on the visual ana- logue scale (VAS) for pain perception at the baseline/start of the treatment
- refractoriness to drugs for pain relief - such as tricyclic antidepressants, antiepileptic drugs, and/or narcot- ics (pain resistant to at least two of these drugs supplied in ade- quate dosages for 6 months)
- informed consent
Exclusion Criteria:
- patients with any clinically significant or unstable medical or progressive neurologic disorder
- contraindication for electrial stimulation such as pacemaker implant
- Women of childbearing age or pregnancy
- significant cognitive deficit
- Syringomyelia
- neuropsychiatric comorbidity
- depressive disorder (as indicated by a score of 10 greater on the Beck Depression Inventory)
- history of substance abuse
- skin defect under the electrodes
- progressive neurological disease or other secondary conditions that could impact neuropathic pain
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Crossover-opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: tsDCS
In the tsDCS group, anodal tsDCS will be applied for 20 minutes.
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Both groups use the same DC-Stimulator Plus (NeuroConn GmbH, Ilmenaus, Germany). In the tsDCS group, anode electrode is placed over tenth thoracic vertebra to target spinal cord with 2mA for 20 min, and the cathode (reference) electrode on the head vertex (in the Cz location according to the 10-20 EEG system) In sham tsDCS group, anode electrode is placed over tenth thoracic vertebra to target spinal cord with 2mA for 30s, and the cathode (reference) electrode on the head vertex (in the Cz location according to the 10-20 EEG system). The current was discontinued after 30 s while the power indicator remained on.
Andere namen:
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Placebo-vergelijker: sham
In sham tsDCS group, the current of anodal tsDCS will be discontinued after 30 s while the power indicator remained on for 20 minutes.
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Both groups use the same DC-Stimulator Plus (NeuroConn GmbH, Ilmenaus, Germany). In the tsDCS group, anode electrode is placed over tenth thoracic vertebra to target spinal cord with 2mA for 20 min, and the cathode (reference) electrode on the head vertex (in the Cz location according to the 10-20 EEG system) In sham tsDCS group, anode electrode is placed over tenth thoracic vertebra to target spinal cord with 2mA for 30s, and the cathode (reference) electrode on the head vertex (in the Cz location according to the 10-20 EEG system). The current was discontinued after 30 s while the power indicator remained on.
Andere namen:
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Numeric rating scale (NRS) for neuropathic pain
Tijdsspanne: Baseline NRS (average NRS over the preceding 24h), Change from Baseline NRS at 0, 60 and 120 minutes after the start of the stimulation
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On a scale of 0 to 10, with 0 being no pain at all and 10 being the worst pain imaginable
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Baseline NRS (average NRS over the preceding 24h), Change from Baseline NRS at 0, 60 and 120 minutes after the start of the stimulation
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Patient Global Assessment (PGA)
Tijdsspanne: Baseline PGA (average PGA over the preceding 24h), Change from Baseline PGA at 0, 60 and 120 minutes after the start of the stimulation
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One of the most widely used patient reported outcomes (PROs) & PGA reflects the global impact of the disease from the patient's perspective
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Baseline PGA (average PGA over the preceding 24h), Change from Baseline PGA at 0, 60 and 120 minutes after the start of the stimulation
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Present Pain Intensity (PPI)
Tijdsspanne: Baseline PPI (average PPI over the preceding 24h), Change from Baseline PPI at 0, 60 and 120 minutes after the start of the stimulation
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Patient's subjective feeling of the intensity of pain right now 0: No pain
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Baseline PPI (average PPI over the preceding 24h), Change from Baseline PPI at 0, 60 and 120 minutes after the start of the stimulation
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Medewerkers en onderzoekers
Publicaties en nuttige links
Algemene publicaties
- Cogiamanian F, Vergari M, Pulecchi F, Marceglia S, Priori A. Effect of spinal transcutaneous direct current stimulation on somatosensory evoked potentials in humans. Clin Neurophysiol. 2008 Nov;119(11):2636-40. doi: 10.1016/j.clinph.2008.07.249. Epub 2008 Sep 10.
- Ngernyam N, Jensen MP, Arayawichanon P, Auvichayapat N, Tiamkao S, Janjarasjitt S, Punjaruk W, Amatachaya A, Aree-uea B, Auvichayapat P. The effects of transcranial direct current stimulation in patients with neuropathic pain from spinal cord injury. Clin Neurophysiol. 2015 Feb;126(2):382-90. doi: 10.1016/j.clinph.2014.05.034. Epub 2014 Jun 21.
- Cogiamanian F, Vergari M, Schiaffi E, Marceglia S, Ardolino G, Barbieri S, Priori A. Transcutaneous spinal cord direct current stimulation inhibits the lower limb nociceptive flexion reflex in human beings. Pain. 2011 Feb;152(2):370-375. doi: 10.1016/j.pain.2010.10.041. Epub 2010 Dec 14.
- Parazzini M, Fiocchi S, Liorni I, Rossi E, Cogiamanian F, Vergari M, Priori A, Ravazzani P. Modeling the current density generated by transcutaneous spinal direct current stimulation (tsDCS). Clin Neurophysiol. 2014 Nov;125(11):2260-2270. doi: 10.1016/j.clinph.2014.02.027. Epub 2014 Apr 3.
Studie record data
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Studie start
Primaire voltooiing (Verwacht)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 1604-007-752 SNUH
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
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Klinische onderzoeken op tsDCS
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The University of Texas Health Science Center,...TIRR Memorial HermannVoltooidRuggengraat letselVerenigde Staten
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The University of Texas Health Science Center,...TIRR/Mission ConnectVoltooidOnvolledige dwarslaesieVerenigde Staten
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VA Office of Research and DevelopmentVoltooid
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Université Catholique de LouvainNog niet aan het werven
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Institut National de la Santé Et de la Recherche...VoltooidPrimaire orthostatische tremorFrankrijk
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Bronx VA Medical CenterNew York State Department of HealthVoltooidRuggenmergletsels | Ruggenmergletsel op C5-C7-niveau | Tetraplegie/tetrapareseVerenigde Staten
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Universidade Federal de PernambucoOnbekend
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The University of Texas Health Science Center,...BeëindigdVerworven hersenletselVerenigde Staten
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Max Planck Research Group Pain PerceptionAanmelden op uitnodiging
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University of FloridaEunice Kennedy Shriver National Institute of Child Health and Human Development... en andere medewerkersActief, niet wervendSCI - Ruggenmergletsel | Onvolledige dwarslaesieVerenigde Staten