Khan Nida, Khan Muhammad Ahmar, Muzaffar Naila, Ismail Ahmad, Ghafoor Abdul, Campbell Jonathon R, Le Coroller Gwenaelle, Nisa Zia Un, Merle Corinne Simone, Khan Muhammad Amir
Association for Social Development, Islamabad, Pakistan.
National TB Control Programme, Islamabad, Pakistan.
BMC Infect Dis. 2025 May 7;25(1):674. doi: 10.1186/s12879-025-11068-1.
Pakistan has one of the largest burdens of rifampicin-resistant/ multidrug-resistant TB according to the global estimates. Novel all oral treatment regimens containing new antibiotics with reduced treatment duration are available. World Health Organization guidelines recommend the use of shorter all-oral regimens under operational research. To guide recommendations, we will compare two all-oral, short (≤ 11 months) regimens for the outcomes of efficacy, safety, cost, and health-related quality of life under programmatic conditions in Pakistan.
This is a stepped wedge, cluster randomized controlled trial with economic evaluation and health related quality of life sub-studies. Modified all-oral 9-month regimen will be sequentially rolled-out compared with the standard all-oral 11-month regimen at 12 sites in Punjab, Islamabad and Azad Jammu and Kashmir region, Pakistan. A total of 400 eligible participants will be enrolled in both study arms. The primary outcome is difference in efficacy as measured by the proportion of patients with treatment success without recurrence at 12 months after the end of treatment between regimens using a non-inferiority design with a margin of 12%. The intention to treat analysis principle will be employed and a marginal mean model with Poisson generalized estimation equations, and a log-link will be used to assess the relative risk. The economic evaluation will be carried out from the healthcare providers perspective; linear mixed models will be used to estimate differences in costs between arms. Health related quality of life will be measured with the EQ-5D-3L quality of life questionnaire at four time points during the study period. The impact will be assessed by calculating the changes for each participant between time points. Ethical approval for this study has been obtained from national bioethics committee, Pakistan (Ref: No.4-87/NBC-491/20/48).
The study's findings will be disseminated to physicians, program implementers, scientific audiences, and policymakers on both a national and international level via reports, presentations, and scientific publications.
ISRCTN registry. ISRCTN17334530, 'retrospectively registered' on 8th February 2021. 'Clinical trial number: not applicable.'
根据全球估计,巴基斯坦是耐利福平/耐多药结核病负担最重的国家之一。目前已有含新抗生素且疗程缩短的新型全口服治疗方案。世界卫生组织指南建议在开展研究时使用疗程更短的全口服方案。为指导相关建议,我们将在巴基斯坦的项目条件下,比较两种全口服、短疗程(≤11个月)方案在疗效、安全性、成本及健康相关生活质量方面的结果。
这是一项带有经济评估和健康相关生活质量子研究的阶梯式楔形整群随机对照试验。在巴基斯坦旁遮普省、伊斯兰堡和查谟和克什米尔地区的12个地点,将改良的全口服9个月方案与标准的全口服11个月方案依次推出。两个研究组共将招募400名符合条件的参与者。主要结局是疗效差异,通过采用非劣效性设计、非劣效界值为12%的方案,比较治疗结束后12个月时治疗成功且无复发的患者比例来衡量。将采用意向性分析原则,使用泊松广义估计方程的边际均值模型和对数链接来评估相对风险。经济评估将从医疗服务提供者的角度进行;线性混合模型将用于估计两组之间的成本差异。在研究期间的四个时间点,将使用EQ-5D-3L生活质量问卷来测量健康相关生活质量。将通过计算每个参与者在各时间点之间的变化来评估影响。本研究已获得巴基斯坦国家生物伦理委员会的伦理批准(参考编号:4-87/NBC-491/20/48)。
该研究的结果将通过报告、演讲和科学出版物在国家和国际层面传播给医生、项目实施者、科学界人士和政策制定者。
ISRCTN注册库。ISRCTN17334530,于2021年2月8日“追溯注册”。“临床试验编号:不适用。”