National Institute for Medical Research (NIMR), Mbeya Medical Research Centre, Mbeya, Tanzania.
Departmentt of Pharmacy, Radboud Institute for Health Sciences, Radboud University Medical Center (RUMC), Nijmegen, The Netherlands.
Trials. 2022 Jun 10;23(1):480. doi: 10.1186/s13063-022-06296-8.
Diabetes mellitus (DM) increases the risk of tuberculosis (TB) and will hamper global TB control due to the dramatic rise in type 2 DM in TB-endemic settings. In this trial, we will examine the efficacy and safety of TB preventive therapy against the development of TB disease in people with DM who have latent TB infection (LTBI), with a 12-week course of rifapentine and isoniazid (3HP).
The 'Prevention of tuberculosis in diabetes mellitus' (PROTID) consortium will randomise 3000 HIV-negative eligible adults with DM and LTBI, as evidenced by a positive tuberculin skin test or interferon gamma release assay, to 12 weeks of 3HP or placebo. Participants will be recruited through screening adult patients attending DM clinics at referral hospitals in Tanzania and Uganda. Patients with previous TB disease or treatment with a rifamycin medication or isoniazid (INH) in the previous 2 years will be excluded. The primary outcome is the occurrence of definite or probable TB disease; secondary outcome measures include adverse events, all-cause mortality and treatment completion. The primary efficacy analysis will be intention-to-treat; per-protocol analyses will also be carried out. We will estimate the ratio of TB incidence rates in intervention and control groups, adjusting for the study site using Poisson regression. Results will be reported as efficacy estimates (1-rate ratio). Cumulative incidence rates allowing for death as a competing risk will also be reported. Approximately 1000 LTBI-negative, HIV-negative participants will be enrolled consecutively into a parallel cohort study to compare the incidence of TB in people with DM who are LTBI negative vs positive. A number of sub-studies will be conducted among others to examine the prevalence of LTBI and active TB, estimate the population impact and cost-effectiveness of LTBI treatment in people living with DM in these African countries and address gaps in the prevention and therapeutic management of combined TB-DM.
PROTID is anticipated to generate key evidence to guide decisions over the use of TB preventive treatment among people with DM as an important target group for better global TB control.
ClinicalTrials.gov NCT04600167 . Registered on 23 October 2020.
糖尿病(DM)会增加结核病(TB)的风险,并且由于结核病流行地区 2 型糖尿病的急剧增加,将阻碍全球结核病控制。在这项试验中,我们将研究利福平吡嗪酰胺(3HP)12 周疗程对潜伏性结核感染(LTBI)的糖尿病患者发生结核病疾病的疗效和安全性。
“糖尿病中的结核病预防”(PROTID)联盟将随机分配 3000 名 HIV 阴性的符合条件的成年糖尿病患者和 LTBI 患者,这些患者的证据为结核菌素皮肤试验或干扰素-γ释放试验阳性,接受 12 周的 3HP 或安慰剂治疗。参与者将通过筛查坦桑尼亚和乌干达转诊医院的糖尿病诊所的成年患者招募。有既往结核病病史或在过去 2 年内使用过利福霉素药物或异烟肼(INH)的患者将被排除。主要结局是确诊或可能的结核病发病;次要结局包括不良事件、全因死亡率和治疗完成情况。主要疗效分析将采用意向治疗;还将进行方案分析。我们将使用泊松回归调整研究地点,估计干预组和对照组的结核病发病率比值。结果将报告为疗效估计值(1-比率比)。还将报告允许死亡作为竞争风险的累积发病率。大约 1000 名 LTBI 阴性、HIV 阴性的参与者将连续纳入平行队列研究,以比较 LTBI 阴性和阳性的糖尿病患者的结核病发病率。还将进行一些子研究,以检查 LTBI 和活动性 TB 的患病率,估计在这些非洲国家中对患有 DM 的人进行 LTBI 治疗的人群影响和成本效益,并解决合并 TB-DM 的预防和治疗管理方面的差距。
PROTID 有望产生关键证据,以指导在糖尿病患者中使用结核病预防性治疗的决策,因为他们是更好的全球结核病控制的重要目标人群。
ClinicalTrials.gov NCT04600167。于 2020 年 10 月 23 日注册。