The Efficacy of Botulinum Toxin in Patients with Cervicogenic Headache: a Placebo-Controlled Clinical Trial
Objective: Botulinum toxin type-A (BoNTA) has been considered a treatment option for CH. The aim of this study was to assess the effectiveness of BoNTA treatment in patients with medically resistant CH.Materials and Methods: Forty patients with CH were included in the study. Patients in the BoNTA gr...
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doaj-c5dbb0f52ac74e83abb42784acac33842020-11-24T21:55:52ZengGalenos Publishing HouseBalkan Medical Journal2146-31232146-31312012-06-01292184187The Efficacy of Botulinum Toxin in Patients with Cervicogenic Headache: a Placebo-Controlled Clinical TrialZeki OdabaşıYaşar KütükçüÜmit Hıdır UlaşBilgin ÖztürkÖmer KaradaşObjective: Botulinum toxin type-A (BoNTA) has been considered a treatment option for CH. The aim of this study was to assess the effectiveness of BoNTA treatment in patients with medically resistant CH.Materials and Methods: Forty patients with CH were included in the study. Patients in the BoNTA group (n=20) were administered 10 U of BoNTA bilaterally to the frontal muscles, 20 U to the temporal muscles, 15 U to the semispinalis capitis, 15 U to the splenius capitis, and 15 U to the trapezius muscles (total: 150 U). Patients in the placebo group (n=20) received 0.2 mL of saline administrated to the same sites. All participations were evaluated 6 and 12 weeks after treatment; side effects, the number of painful days, severity (by visual analogue scale, VAS) and frequency of pain were evaluated.Results: In the BoNTA group, the severity and frequency of pain 6 and 12 weeks post treatment were significantly lower than pre-treatment levels (p<0.05). At 12 weeks post treatment, the severity and frequency of pain in the BoNTA group were lower than in the placebo group (p<0.05). Conclusion: The findings suggest that BoNTA was an effective treatment for CH. http://balkanmedicaljournal.org/text.php3?id=859Cervicogenic headacheBotulinum toxin A |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zeki Odabaşı Yaşar Kütükçü Ümit Hıdır Ulaş Bilgin Öztürk Ömer Karadaş |
spellingShingle |
Zeki Odabaşı Yaşar Kütükçü Ümit Hıdır Ulaş Bilgin Öztürk Ömer Karadaş The Efficacy of Botulinum Toxin in Patients with Cervicogenic Headache: a Placebo-Controlled Clinical Trial Balkan Medical Journal Cervicogenic headache Botulinum toxin A |
author_facet |
Zeki Odabaşı Yaşar Kütükçü Ümit Hıdır Ulaş Bilgin Öztürk Ömer Karadaş |
author_sort |
Zeki Odabaşı |
title |
The Efficacy of Botulinum Toxin in Patients with Cervicogenic Headache: a Placebo-Controlled Clinical Trial |
title_short |
The Efficacy of Botulinum Toxin in Patients with Cervicogenic Headache: a Placebo-Controlled Clinical Trial |
title_full |
The Efficacy of Botulinum Toxin in Patients with Cervicogenic Headache: a Placebo-Controlled Clinical Trial |
title_fullStr |
The Efficacy of Botulinum Toxin in Patients with Cervicogenic Headache: a Placebo-Controlled Clinical Trial |
title_full_unstemmed |
The Efficacy of Botulinum Toxin in Patients with Cervicogenic Headache: a Placebo-Controlled Clinical Trial |
title_sort |
efficacy of botulinum toxin in patients with cervicogenic headache: a placebo-controlled clinical trial |
publisher |
Galenos Publishing House |
series |
Balkan Medical Journal |
issn |
2146-3123 2146-3131 |
publishDate |
2012-06-01 |
description |
Objective: Botulinum toxin type-A (BoNTA) has been considered a treatment option for CH. The aim of this study was to assess the effectiveness of BoNTA treatment in patients with medically resistant CH.Materials and Methods: Forty patients with CH were included in the study. Patients in the BoNTA group (n=20) were administered 10 U of BoNTA bilaterally to the frontal muscles, 20 U to the temporal muscles, 15 U to the semispinalis capitis, 15 U to the splenius capitis, and 15 U to the trapezius muscles (total: 150 U). Patients in the placebo group (n=20) received 0.2 mL of saline administrated to the same sites. All participations were evaluated 6 and 12 weeks after treatment; side effects, the number of painful days, severity (by visual analogue scale, VAS) and frequency of pain were evaluated.Results: In the BoNTA group, the severity and frequency of pain 6 and 12 weeks post treatment were significantly lower than pre-treatment levels (p<0.05). At 12 weeks post treatment, the severity and frequency of pain in the BoNTA group were lower than in the placebo group (p<0.05). Conclusion: The findings suggest that BoNTA was an effective treatment for CH. |
topic |
Cervicogenic headache Botulinum toxin A |
url |
http://balkanmedicaljournal.org/text.php3?id=859 |
work_keys_str_mv |
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