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成人结核性脑膜炎强化短程方案与标准方案的比较评价:一项开放标签、多中心、平行臂、随机对照优效性试验(INSHORT 试验)方案。

Comparative evaluation of intensified short course regimen and standard regimen for adults TB meningitis: a protocol for an open label, multi-center, parallel arms, randomized controlled superiority trial (INSHORT trial).

机构信息

Department of Clinical Research, ICMR- National Institute for Research in Tuberculosis, Chethpet, Chennai, 600031, India.

Department of Infectious Diseases, Christian Medical College, Vellore, India.

出版信息

Trials. 2024 May 2;25(1):294. doi: 10.1186/s13063-024-08133-6.

Abstract

BACKGROUND

Despite several incremental improvements in the management of tuberculous meningitis (TBM), the mortality rates remain high. In spite of national and international guidelines, variation in the choice, dose, and duration of drugs exist between countries and clinicians. We propose to evaluate a shorter and more effective regimen containing agents with augmented intracerebral drug exposure and anti-inflammatory approaches to improve disability-free survival among patients with TBM. Our strategy incorporates the various developments in the field of TBM over the last two decades and only few trials have evaluated a composite of these strategies in the overall outcomes of TBM.

METHODS

An open label, parallel arms, randomized controlled superiority trial will be conducted among 372 participants across 6 sites in India. Eligible participants will be randomly allocated in 1:1:1 ratio into one of the three arms. The intervention arm consists of 2 months of high-dose rifampicin (25 mg/kg), moxifloxacin (400 mg), pyrazinamide, isoniazid, aspirin (150 mg), and steroids followed by rifampicin, isoniazid, and pyrazinamide for 4 months. The second intervention arm includes all the drugs as per the first arm except aspirin and the patients in the control arm will receive treatment according to the National TB Elimination Program guidelines. All participants will be followed up for 1 year after the treatment.  DISCUSSION: Current WHO regimens have agents with poor central nervous system drug exposure and is too long. It does not reflect the accumulating evidence in the field. We propose a comprehensive clinical trial incorporating the emerging evidence accrued over the last two decades to shorten the duration and improve the treatment outcomes. This multi-centric trial may generate crucial evidence with policy and practice implications in the treatment of TBM.

TRIAL REGISTRATION

Clinical Trial Registry India CTRI/2023/05/053314. Registered on 31 May 2023 ( https://ctri.nic.in/Clinicaltrials/pmaindet2.php?EncHid=ODYzMzg=&Enc=&userName=CTRI/2023/05/053314 ).

CLINICALTRIALS

gov NCT05917340. Registered on 6 August 2023 ( https://classic.

CLINICALTRIALS

gov/ct2/show/NCT05917340 ).

PROTOCOL VERSION

Version 1.3 dated 12 July 2023.

摘要

背景

尽管在结核性脑膜炎(TBM)的治疗方面取得了一些渐进式的改进,但死亡率仍然很高。尽管有国家和国际指南,但各国和临床医生在药物的选择、剂量和疗程方面存在差异。我们建议评估一种更短、更有效的方案,该方案包含具有增强颅内药物暴露的药物和抗炎方法,以提高 TBM 患者的无残疾生存。我们的策略结合了过去二十年 TBM 领域的各项发展,只有少数试验评估了这些策略的组合在 TBM 的总体结果中的作用。

方法

在印度的 6 个地点将进行一项开放标签、平行臂、随机对照优效性试验,共有 372 名参与者符合条件。合格的参与者将按照 1:1:1 的比例随机分配到三个组之一。干预组包括 2 个月的高剂量利福平(25mg/kg)、莫西沙星(400mg)、吡嗪酰胺、异烟肼、阿司匹林(150mg)和类固醇,随后再用利福平、异烟肼和吡嗪酰胺治疗 4 个月。第二个干预组包含除了阿司匹林以外的所有药物,对照组将按照国家结核病消除计划指南进行治疗。所有参与者在治疗后将随访 1 年。

讨论

目前的世卫组织方案中,药物对中枢神经系统的药物暴露效果不佳,且疗程过长。它没有反映该领域不断积累的证据。我们提出了一项综合临床试验,纳入了过去二十年中积累的新证据,以缩短疗程并改善治疗结果。这项多中心试验可能会产生具有政策和实践意义的关键证据,对 TBM 的治疗产生影响。

试验注册

印度临床试验注册中心 CTRI/2023/05/053314。于 2023 年 5 月 31 日注册(https://ctri.nic.in/Clinicaltrials/pmaindet2.php?EncHid=ODYzMzg=&Enc=&userName=CTRI/2023/05/053314)。

临床试验

gov NCT05917340。于 2023 年 8 月 6 日注册(https://classic.clinicaltrials.gov/ct2/show/NCT05917340)。

方案版本

2023 年 7 月 12 日第 1.3 版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f25a/11064413/994f177f8790/13063_2024_8133_Fig1_HTML.jpg

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