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...

Full description

Bibliographic Details
Main Authors: Zeki Odabaşı, Yaşar Kütükçü, Ümit Hıdır Ulaş, Bilgin Öztürk, Ömer Karadaş
Format: Article
Language:English
Published: Galenos Publishing House 2012-06-01
Series:Balkan Medical Journal
Subjects:
Online Access:http://balkanmedicaljournal.org/text.php3?id=859
id doaj-c5dbb0f52ac74e83abb42784acac3384
record_format Article
spelling 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 AT zekiodabası theefficacyofbotulinumtoxininpatientswithcervicogenicheadacheaplacebocontrolledclinicaltrial
AT yasarkutukcu theefficacyofbotulinumtoxininpatientswithcervicogenicheadacheaplacebocontrolledclinicaltrial
AT umithıdırulas theefficacyofbotulinumtoxininpatientswithcervicogenicheadacheaplacebocontrolledclinicaltrial
AT bilginozturk theefficacyofbotulinumtoxininpatientswithcervicogenicheadacheaplacebocontrolledclinicaltrial
AT omerkaradas theefficacyofbotulinumtoxininpatientswithcervicogenicheadacheaplacebocontrolledclinicaltrial
AT zekiodabası efficacyofbotulinumtoxininpatientswithcervicogenicheadacheaplacebocontrolledclinicaltrial
AT yasarkutukcu efficacyofbotulinumtoxininpatientswithcervicogenicheadacheaplacebocontrolledclinicaltrial
AT umithıdırulas efficacyofbotulinumtoxininpatientswithcervicogenicheadacheaplacebocontrolledclinicaltrial
AT bilginozturk efficacyofbotulinumtoxininpatientswithcervicogenicheadacheaplacebocontrolledclinicaltrial
AT omerkaradas efficacyofbotulinumtoxininpatientswithcervicogenicheadacheaplacebocontrolledclinicaltrial
_version_ 1725860979815743488