Pilot study evaluating treatment with sumatriptan for moderate to severe post-traumatic headache: A phase 2 open-label study.

IF 5.4 2区 医学 Q1 CLINICAL NEUROLOGY Headache Pub Date : 2024-10-01 Epub Date: 2024-08-13 DOI:10.1111/head.14807
Tara L Sharma, Sylvia Lucas, Jason Barber, Jeanne M Hoffman
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Abstract

Objective: Our primary outcome was to determine the feasibility of patients with post-traumatic headache (PTH) keeping a daily headache diary and using sumatriptan as directed. Secondary outcomes include determining if sumatriptan is effective in aborting PTH and whether headache resolution is dependent on PTH phenotype.

Background: PTH is prevalent and persistent after traumatic brain injury, yet there have been few studies evaluating the effects of pharmacological treatments in individuals with PTH.

Methods: This is a single-arm, prospective, non-randomized phase 2 clinical trial registered at Clinicaltrials.gov (NCT01854385) and conducted from 2013 to 2017. Data analysis was completed in 2022. Of the 299 participants screened, 40 were enrolled in the study. Participants kept a headache diary documenting headache characteristics and severity. Headache characteristics were used to determine PTH phenotypes of migraine-like, probable migraine-like, or non-migraine-like. Participants reported whether sumatriptan was used for their headache, their response to the medication, if a second dose was taken, and their response to the second dose.

Results: A total of 15 participants out of the 40 enrolled (mean [SD] age, 41.9 [14.2] years, and 53% [21/40] male), met the criteria for the use of sumatriptan, and completed all assessments. Average headache diary compliance rate for the final month of the study was 80% (372/465). While sumatriptan was used for only 19% (122/654) of all reported headaches, 72% (88/122) of those headaches resolved within 2 h of taking the medication. Resolution of headaches with sumatriptan was not significantly different among headache phenotypes (migraine-like: 22/38 [58%], probable migraine-like: 24/29 [83%], non-migraine-like: 6/15 [40%]; p = 0.154).

Conclusions: A daily headache diary is feasible for tracking headache symptoms. Preliminary results also suggest that sumatriptan, a migraine-specific medication, may be beneficial for the treatment of PTH of different clinical phenotypes. Future studies, such as a phase 3 clinical trial with a larger sample size, are needed to better understand the efficacy of sumatriptan in the treatment of PTH.

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评估舒马曲普坦治疗中重度创伤后头痛的试点研究:2期开放标签研究。
目的:我们的主要研究结果是确定创伤后头痛(PTH)患者坚持每天写头痛日记并遵医嘱使用舒马曲普坦的可行性。次要结果包括确定舒马曲普坦是否能有效中止 PTH,以及头痛的缓解是否取决于 PTH 的表型:背景:PTH 在脑外伤后普遍存在并持续存在,但很少有研究评估药物治疗对 PTH 患者的影响:这是一项单臂、前瞻性、非随机的2期临床试验,已在Clinicaltrials.gov(NCT01854385)注册,于2013年至2017年进行。数据分析于 2022 年完成。在筛选出的 299 名参与者中,有 40 人参加了研究。参与者记录头痛日记,记录头痛特征和严重程度。头痛特征用于确定偏头痛样、可能偏头痛样或非偏头痛样的 PTH 表型。参与者报告是否使用舒马曲普坦治疗头痛、对药物的反应、是否服用第二剂以及对第二剂的反应:在 40 名参与者中,共有 15 人(平均 [SD] 年龄为 41.9 [14.2] 岁,53% [21/40] 为男性)符合使用舒马曲普坦的标准,并完成了所有评估。研究最后一个月的平均头痛日记达标率为 80%(372/465)。在所有报告的头痛中,只有19%(122/654)的人使用了舒马曲普坦,但其中72%(88/122)的头痛在服药后2小时内缓解。22/38[58%],可能偏头痛:24/29[83%],非偏头痛:结论:结论:每日头痛日记可用于追踪头痛症状。初步结果还表明,偏头痛特异性药物舒马曲普坦可能有利于治疗不同临床表型的PTH。为了更好地了解舒马曲普坦治疗PTH的疗效,今后还需要进行更多的研究,如样本量更大的3期临床试验。
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来源期刊
Headache
Headache 医学-临床神经学
CiteScore
9.40
自引率
10.00%
发文量
172
审稿时长
3-8 weeks
期刊介绍: Headache publishes original articles on all aspects of head and face pain including communications on clinical and basic research, diagnosis and management, epidemiology, genetics, and pathophysiology of primary and secondary headaches, cranial neuralgias, and pains referred to the head and face. Monthly issues feature case reports, short communications, review articles, letters to the editor, and news items regarding AHS plus medicolegal and socioeconomic aspects of head pain. This is the official journal of the American Headache Society.
期刊最新文献
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