2002
DOI: 10.1007/s101940200024
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Physical therapy and adjunctive botulinum toxin type A in the treatment of cervical headache: a double-blind, randomised, placebo-controlled study

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Cited by 26 publications
(21 citation statements)
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“…One study [18] showed a significant improvement in terms of VAS and range of movement; however, there was a significant difference in pre-injection levels (baseline VAS: score saline: 3; baseline VAS score BoNT/A: 6.5). In the other trial BoNT/A was given as add-on to physical therapy [26]. Although headache severity, headache-free days and headache hours improved significantly in both groups, only a trend in favor of BoNT/A was observable.…”
Section: ■ Cervicogenic Headachementioning
confidence: 86%
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“…One study [18] showed a significant improvement in terms of VAS and range of movement; however, there was a significant difference in pre-injection levels (baseline VAS: score saline: 3; baseline VAS score BoNT/A: 6.5). In the other trial BoNT/A was given as add-on to physical therapy [26]. Although headache severity, headache-free days and headache hours improved significantly in both groups, only a trend in favor of BoNT/A was observable.…”
Section: ■ Cervicogenic Headachementioning
confidence: 86%
“…This difference was reported to be significant. Schnider [26] studied 33 patients with cervicogenic headache according to the IHS criteria. Ninety MU Botox® or saline were injected in addition to standardized physical therapy.…”
Section: ■ Cervicogenic Headachementioning
confidence: 99%
“…However, there are only a few case reports on BoNTA treatment for cluster headache, and overall the results have been inconsistent (32). Despite the fact that in Schnider et al's randomized, double-blind placebo-controlled study there was no significant difference in the severity of pain between the BoNTA and placebo groups, the duration of pain in the BoNTA group decreased (31).…”
Section: Discussionmentioning
confidence: 99%
“…Botulinum toxin-A versus placebo for chronic cervicogenic headache pain (2 trials 58 participants [53, 54] and disability (1 trial [53]) at short-term and 1 trial [53] at intermediate-term follow-up. Additionally botulinum toxin-A versus placebo (saline) (1 trial [55], 45 participants) was not beneficial in improving disability or global perceived effect for chronic myofascial neck and shoulder pain at intermediate-term follow-up.…”
Section: Evidence Of No Benefitmentioning
confidence: 99%