Open-label, Multicenter, Randomized Study Investigating the Efficacy and Safety of Botulinum Toxin Type A in the Treatment of Myofascial Pain Syndrome in the Neck and Shoulder Girdle

2012 ◽  
Vol 20 (2) ◽  
pp. 95-99 ◽  
Author(s):  
Jörg Jerosch ◽  
Manfred Söhling
2007 ◽  
Vol 65 (3a) ◽  
pp. 596-598 ◽  
Author(s):  
Carla Menezes ◽  
Bernardo Rodrigues ◽  
Elza Magalhães ◽  
Ailton Melo

Botulinum toxin type A (BT-A) has been described as an important strategy to various types of pain such as cervical dystonia, myofascial pain syndrome and headache. Although BT-A efficacy has not been proven in tension type headache, its use in migraine continues controversial. In this open trial, we evaluated the efficacy of BT-A in refractory migraine. BT-A was injected in patients diagnosed with migraine who had previously used three classes of prophylactic drugs by at least one year with no response. The most important improvement was observed within 30 days, but pain intensity and frequency of headache had been decreased until the end of three months of follow up. Side effects of BT-A were mild and self limited. We conclude that BT-A seems to be a safe and effective treatment to refractory migraine patients.


Toxins ◽  
2020 ◽  
Vol 13 (1) ◽  
pp. 6
Author(s):  
Jose-Francisco Montes-Carmona ◽  
Luis-Miguel Gonzalez-Perez ◽  
Pedro Infante-Cossio

Botulinum toxin type A (BTA) injection is considered an available alternative treatment for myofascial pain. However, its efficacy in treating masticatory myofascial pain syndrome (MMPS) remains unclear. The purpose of this study was to evaluate whether the BTA injection into the affected muscles would significantly reduce pain and improve function, and to assess its efficacy, safety, and therapeutic indications in a randomized, single-center clinical trial. Sixty patients with MMPS were randomized into three groups evenly to receive a single session injection of saline solution (SS group), lidocaine (LD group), and BTA (BTA group) in the masseter, temporal, and pterygoid muscles after an electromyographic study. Patients’ pain was classified as localized or referred according to the DC/TMD classification. Assessments were performed on pre-treatment, and subsequently, on days 7, 14, 28, 60, 90, and 180. A significant reduction in pain and improvement of mandibular movements was found in the BTA group compared to the SS and LD groups. The response lasted until day 180 and was more intense in patients with localized myalgia and focused myofascial pain than in referred remote pain. No significant adverse reactions were observed. A single BTA injection can be considered an effective treatment option in patients with localized MMPS by reducing pain and improving mandibular movements, which persisted up to 6 months.


2021 ◽  
Author(s):  
Gabriel Cerqueira Santos ◽  
Caio de Almeida Lellis ◽  
Bruno Coelho Duarte Oliveira ◽  
Letícia Romeira Belchior ◽  
Caíque Seabra Garcia de Menezes Figueiredo ◽  
...  

Introduction: Myofascial pain syndrome (MPS) is a regional painful condition characterized by the presence of trigger points in the affected muscles, and botulinum toxin type A (BoNT-A) is a possible therapeutic option. Objectives: To evaluate the safety and efficacy of botulinum toxin in the management of MSD. Design and setting: A systematic review conducted at the Pontifical Catholic University of Goiás. Methodology: A systematic review was conducted in the PubMed, IBECS and VHL databases: “(Myofascial Pain Syndromes OR Myofascial Trigger Point Pain) AND Botulinum toxin”. Randomized studies, clinical trials and case reports published in the last 10 years were selected. Results: Two randomized trials concluded that application of BoNT-A, regard less of the application site, did not show significant improvement in pain intensity compared to the control group. Also, another multicenter, random ized trial reported that application of ToNB-A to the masseter muscles did not result in improvement of SDM within three months of application. Finally, a clinical trial reported improvement in visual numeric scores of myofascial pain in the scapular girdle in subjects who received a second dose (P = 0.019). Conclusion: BoNT-A was not effective in improving SDM at any site of ap plication and in any dosage studied, except in a single study, therefore insuf ficient to state whether subsequent doses have better results.


Author(s):  
Marina I. Soykher ◽  
O. R Orlova ◽  
L. R Mingazova ◽  
M. G Soykher ◽  
A. A Mammedov

Treatment of diseases of the temporomandibular joint (TMJ), complicated by hypertension of the masticatory muscles, remains one of the unsolved problems of dentistry. The purpose of this clinical study is to assess the safety and efficacy of the first Russian botulinum toxin a (BTA) Relatox® for the correction of masticatory muscle hypertension in patients with myofascial pain syndrome, as well as its comparison with the Lantox® by these parameters. Injections of botulinum toxin type A are a method of treatment in patients with myofascial facial pain syndrome with high therapeutic potential. The analysis of clinical results of using the Russian botulinum toxin type A of Relatox® shows high clinical efficacy. Comparative analysis of Lantox® and Relatox® showed no differences in safety and efficacy.


2016 ◽  
Vol 147 (12) ◽  
pp. 959-973.e1 ◽  
Author(s):  
Mohammad Khalifeh ◽  
Kalpesh Mehta ◽  
Nibu Varguise ◽  
Piedad Suarez-Durall ◽  
Reyes Enciso

2014 ◽  
Vol 27 (4) ◽  
pp. 485-492 ◽  
Author(s):  
Juan Avendaño-Coy ◽  
Julio Gómez-Soriano ◽  
Marta Valencia ◽  
Jesús Estrada ◽  
Francisco Leal ◽  
...  

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