Design and implementation of botulinum toxin on cricopharyngeal dysfunction guided by a combination of catheter balloon, ultrasound, and electromyography (BECURE) in patients with stroke: study protocol for a randomized, double-blinded, placebo-controlled trial

被引:8
|
作者
Xie, Mengshu [1 ]
Dou, Zulin [1 ]
Wan, Guifang [1 ]
Zeng, Peishan [1 ]
Wen, Hongmei [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Rehabil Med, 600 Tianhe Rd, Guangzhou 510630, Guangdong, Peoples R China
关键词
Botulinum toxin; Clinical trial; Cricopharyngeal achalasia; Cricopharyngeal dysfunction; Dysphagia; Protocol; Rehabilitation;
D O I
10.1186/s13063-021-05195-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Cricopharyngeal dysfunction (CPD) occurs in various neurological disorders, especially stroke. The treatment approaches of CPD include swallowing training, cricopharyngeal dilation, botulinum toxin (BTX) injection, and cricopharyngeal myotomy. BTX injection into the cricopharyngeal muscle is effective and safe for some patients with dysphagia, with a success rate between 43 and 100% (mean = 76%). However, well-designed randomized controlled clinical trials are needed to verify its efficacy and safety for the treatment of CPD. The objective of this study is to explore the efficacy and safety of BTX for neurogenic cricopharyngeal achalasia, when administering an injection into the cricopharyngeal muscle guided by a novel precise positioning method, that combines ultrasound, catheter balloon, and electromyography (BECURE). Methods: BECURE is a single-center randomized, placebo controlled, double-blinded, superiority clinical trial. To detect a significant difference between the 2 groups, a sample size of 44 patients is estimated. The intervention is BTX versus placebo, with 1:1 randomization. The randomization sequence from 1 to 44 was generated using the Statistical Package for Social Sciences. The study is divided into two phases. In the first phase, patients will be injected with BTX or the placebo. In the second phase, patients who received a placebo injection and those who did not respond to the first BTX injection will receive an injection of BTX. The primary outcome is the score of the Functional Oral Intake Scale (FOIS). The secondary outcomes are as follows: upper esophageal sphincter (UES) residual pressure, UES resting pressure, duration of UES relaxation, velopharyngeal and laryngopharyngeal peak pressure, UES opening, pharyngeal construction ratio, residue of bolus in the epiglottis valley or piriform sinus, and penetration and aspiration. Discussion: Dysphagia is a common complication of stroke. There is lack of high-quality evidence for the efficacy of BTX in treating neurogenic CPD. This study will clarify whether BTX injection into the cricopharyngeal muscle can be effective and safe for patients with stroke and CPD.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] Design and implementation of botulinum toxin on cricopharyngeal dysfunction guided by a combination of catheter balloon, ultrasound, and electromyography (BECURE) in patients with stroke: study protocol for a randomized, double-blinded, placebo-controlled trial
    Mengshu Xie
    Zulin Dou
    Guifang Wan
    Peishan Zeng
    Hongmei Wen
    Trials, 22
  • [2] Botulinum toxin type A for cephalic cutaneous allodynia in chronic migraine: a randomized, double-blinded, placebo-controlled trial
    Hollanda, Luciano
    Monteiro, Larissa
    Melo, Ailton
    NEUROLOGY INTERNATIONAL, 2014, 6 (04) : 70 - 73
  • [3] Intra-articular botulinum toxin A for refractory shoulder pain: a randomized, double-blinded, placebo-controlled trial
    Singh, Jasvinder A.
    Mahowald, Maren L.
    Noorbaloochi, Siamak
    TRANSLATIONAL RESEARCH, 2009, 153 (05) : 205 - 216
  • [4] A double-blinded, randomized, placebo-controlled pilot study of the safety and efficacy of myobloc (Botulinum toxin type B)-purified neurotoxin complex for the treatment of crow's feet: A double-blinded, placebo-controlled trial
    Baumann, L
    Slezinger, A
    Vujevich, J
    Halem, M
    Bryde, J
    Black, L
    Duncan, R
    DERMATOLOGIC SURGERY, 2003, 29 (05) : 508 - 515
  • [5] Effect of Febuxostat on the Endothelial Dysfunction in Hemodialysis Patients: A Randomized, Placebo-Controlled, Double-Blinded Study
    Alshahawey, Mona
    Shahin, Sara Mahmoud
    Elsaid, Tamer Wahid
    Sabri, Nagwa Ali
    AMERICAN JOURNAL OF NEPHROLOGY, 2017, 45 (05) : 452 - 459
  • [6] Ruyi Zhenbao Pills for Patients with Motor and Sensory Dysfunction after Stroke: A Double-Blinded, Randomized Placebo-Controlled Clinical Trial
    Shan-shan Ling
    Rui-huan Pan
    Le-chang Zhan
    Mei Li
    Zhi-jing Yang
    Hao-dong Yang
    Hong-xia Chen
    Chinese Journal of Integrative Medicine, 2022, 28 : 872 - 878
  • [7] Ruyi Zhenbao Pills for Patients with Motor and Sensory Dysfunction after Stroke: A Double-Blinded, Randomized Placebo-Controlled Clinical Trial
    LING Shanshan
    PAN Ruihuan
    ZHAN Lechang
    LI Mei
    YANG Zhijing
    YANG Haodong
    CHEN Hongxia
    Chinese Journal of Integrative Medicine , 2022, (10) : 872 - 878
  • [8] Ruyi Zhenbao Pills for Patients with Motor and Sensory Dysfunction after Stroke: A Double-Blinded, Randomized Placebo-Controlled Clinical Trial
    LING Shan-shan
    PAN Rui-huan
    ZHAN Le-chang
    LI Mei
    YANG Zhi-jing
    YANG Hao-dong
    CHEN Hong-xia
    Chinese Journal of Integrative Medicine, 2022, 28 (10) : 872 - 878
  • [9] The efficacy of resveratrol in controlling hypertension: study protocol for a randomized, crossover, double-blinded, placebo-controlled trial
    Ali Movahed
    Afshin Ostovar
    Daryoush Iranpour
    Sijo Joseph Thandapilly
    Pema Raj
    Xavier Lieben Louis
    James Michael Smoliga
    Thomas Netticadan
    Trials, 17
  • [10] Ruyi Zhenbao Pills for Patients with Motor and Sensory Dysfunction after Stroke: A Double-Blinded, Randomized Placebo-Controlled Clinical Trial
    Ling Shan-shan
    Pan Rui-huan
    Zhan Le-chang
    Li Mei
    Yang Zhi-jing
    Yang Hao-dong
    Chen Hong-xia
    CHINESE JOURNAL OF INTEGRATIVE MEDICINE, 2022, 28 (10) : 872 - 878