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Kinetic Oscillation Stimulation as Treatment of Acute Migraine: A Randomized, Controlled Pilot Study

OBJECTIVE: To assess the relief of migraine pain, especially in the acute phase, by comparing active treatment, ie, kinetic oscillation stimulation (KOS) in the nasal cavity, with placebo. BACKGROUND: Exploratory trials testing the efficacy of KOS on migraine patients indicated that this treatment c...

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Autores principales: Juto, Jan-Erik, Hallin, Rolf G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4312979/
https://www.ncbi.nlm.nih.gov/pubmed/25546476
http://dx.doi.org/10.1111/head.12485
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author Juto, Jan-Erik
Hallin, Rolf G
author_facet Juto, Jan-Erik
Hallin, Rolf G
author_sort Juto, Jan-Erik
collection PubMed
description OBJECTIVE: To assess the relief of migraine pain, especially in the acute phase, by comparing active treatment, ie, kinetic oscillation stimulation (KOS) in the nasal cavity, with placebo. BACKGROUND: Exploratory trials testing the efficacy of KOS on migraine patients indicated that this treatment could be a fast-acting remedy for acute migraine pain. METHOD: Thirty-six patients were randomized 1:1 using a placebo module to active or placebo treatment in this double-blinded parallel design study. Treatment was administered with a minimally invasive inflatable tip oscillating catheter. Symptom scores (0–10 visual analog scale) were obtained before treatment, every 5 minutes during treatment, at 15 minutes, 2, and 24 hours post-treatment, as well as daily (0–3 migraine pain scale) from 30 days pretreatment until Day 60 post. Thirty-five patients were evaluated (active n = 18, placebo n = 17). The primary end-point was the change in average pain score from before treatment to 15 minutes after treatment. RESULTS: Patients who received active treatment reported reduced pain, eg, average visual analog scale pain scores fell from 5.5 before treatment to 1.2 15 minutes after, while the corresponding scores for recipients of placebo fell from 4.9 to 3.9. The changes in pain scores differed between the 2 treatments by 3.3 points (95% confidence interval: 2.3, 4.4), P < .001. Already 5 minutes into the treatment, the difference (1.9 points) was significant (P = .007). The difference was likewise significant at 2 hours post-treatment (3.7 points, P < .001). One patient experienced an adverse event (a vasovagal reaction with full spontaneous recovery) during placebo treatment. CONCLUSION: KOS is an effective and safe treatment for acute migraine pain.
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spelling pubmed-43129792015-02-10 Kinetic Oscillation Stimulation as Treatment of Acute Migraine: A Randomized, Controlled Pilot Study Juto, Jan-Erik Hallin, Rolf G Headache Research Submissions OBJECTIVE: To assess the relief of migraine pain, especially in the acute phase, by comparing active treatment, ie, kinetic oscillation stimulation (KOS) in the nasal cavity, with placebo. BACKGROUND: Exploratory trials testing the efficacy of KOS on migraine patients indicated that this treatment could be a fast-acting remedy for acute migraine pain. METHOD: Thirty-six patients were randomized 1:1 using a placebo module to active or placebo treatment in this double-blinded parallel design study. Treatment was administered with a minimally invasive inflatable tip oscillating catheter. Symptom scores (0–10 visual analog scale) were obtained before treatment, every 5 minutes during treatment, at 15 minutes, 2, and 24 hours post-treatment, as well as daily (0–3 migraine pain scale) from 30 days pretreatment until Day 60 post. Thirty-five patients were evaluated (active n = 18, placebo n = 17). The primary end-point was the change in average pain score from before treatment to 15 minutes after treatment. RESULTS: Patients who received active treatment reported reduced pain, eg, average visual analog scale pain scores fell from 5.5 before treatment to 1.2 15 minutes after, while the corresponding scores for recipients of placebo fell from 4.9 to 3.9. The changes in pain scores differed between the 2 treatments by 3.3 points (95% confidence interval: 2.3, 4.4), P < .001. Already 5 minutes into the treatment, the difference (1.9 points) was significant (P = .007). The difference was likewise significant at 2 hours post-treatment (3.7 points, P < .001). One patient experienced an adverse event (a vasovagal reaction with full spontaneous recovery) during placebo treatment. CONCLUSION: KOS is an effective and safe treatment for acute migraine pain. BlackWell Publishing Ltd 2015-01 2014-12-29 /pmc/articles/PMC4312979/ /pubmed/25546476 http://dx.doi.org/10.1111/head.12485 Text en © 2014 The Authors. Headache published by Wiley Periodicals, Inc. on behalf of American Headache Society. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Research Submissions
Juto, Jan-Erik
Hallin, Rolf G
Kinetic Oscillation Stimulation as Treatment of Acute Migraine: A Randomized, Controlled Pilot Study
title Kinetic Oscillation Stimulation as Treatment of Acute Migraine: A Randomized, Controlled Pilot Study
title_full Kinetic Oscillation Stimulation as Treatment of Acute Migraine: A Randomized, Controlled Pilot Study
title_fullStr Kinetic Oscillation Stimulation as Treatment of Acute Migraine: A Randomized, Controlled Pilot Study
title_full_unstemmed Kinetic Oscillation Stimulation as Treatment of Acute Migraine: A Randomized, Controlled Pilot Study
title_short Kinetic Oscillation Stimulation as Treatment of Acute Migraine: A Randomized, Controlled Pilot Study
title_sort kinetic oscillation stimulation as treatment of acute migraine: a randomized, controlled pilot study
topic Research Submissions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4312979/
https://www.ncbi.nlm.nih.gov/pubmed/25546476
http://dx.doi.org/10.1111/head.12485
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