Effectiveness and safety of shortened intensive treatment for children with tuberculous meningitis (SURE): a protocol for a phase 3 randomised controlled trial evaluating 6 months of antituberculosis therapy and 8 weeks of aspirin in Asian and African children with tuberculous meningitis.

Julie Huynh ORCID logo ; Chishala Chabala ; Suvasini Sharma ; Louise Choo ; Varinder Singh ; Naveen Sankhyan ; Hilda Mujuru ; Nhung Nguyen ; Tung Huu Trinh ; Phuc Huu Phan ; +23 more... Nguyen Viet Nhung ; Kafula Lisa Nkole ; Titiksha Sirari ORCID logo ; Constantine Mutata ; Elena Frangou ; Anna Griffiths ; Eric Wobudeya ; Caitlin Muller ; Sierra Santana ; Evelyne Kestelyn ; Lam Van Nguyen ; Thanh Nguyen ; Dai Tran ; James A Seddon ; Anna Turkova ORCID logo ; Susan Abarca-Salazar ; Robin Basu-Roy ; Guy E Thwaites ; Angela Crook ; Suzanne T Anderson ; Diana M Gibb ; SURE trial team ; Trial team SURE ; (2025) Effectiveness and safety of shortened intensive treatment for children with tuberculous meningitis (SURE): a protocol for a phase 3 randomised controlled trial evaluating 6 months of antituberculosis therapy and 8 weeks of aspirin in Asian and African children with tuberculous meningitis. BMJ open, 15 (4). e088543. ISSN 2044-6055 DOI: 10.1136/bmjopen-2024-088543
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INTRODUCTION: Childhood tuberculous meningitis (TBM) is a devastating disease. The long-standing WHO recommendation for treatment is 2 months of intensive phase with isoniazid (H), rifampicin (R), pyrazinamide (Z) and ethambutol (E), followed by 10 months of isoniazid and rifampicin. In 2022, WHO released a conditional recommendation that 6 months of intensified antituberculosis therapy (ATT) could be used as an alternative for drug-susceptible TBM. However, this has never been evaluated in a randomised clinical trial. Trials evaluating ATT shortening regimens using high-dose rifampicin and drugs with better central nervous system penetration alongside adjuvant anti-inflammatory therapy are needed to improve outcomes.

METHODS AND ANALYSIS: The Shortened Intensive Therapy for Children with Tuberculous Meningitis (SURE) trial is a phase 3, randomised, partially blinded, factorial trial being conducted in Asia (India and Vietnam) and Africa (Uganda, Zambia and Zimbabwe). It is coordinated by the Medical Research Council Clinical Trial Unit at University College London (MRCCTU at UCL). 400 children (aged 29 days to <18 years) with clinically diagnosed TBM will be randomised, using a factorial design, to either a 24-week intensified regimen (isoniazid (20 mg/kg), rifampicin (30 mg/kg), pyrazinamide (40 mg/kg) and levofloxacin (20 mg/kg)) or the standard 48-week ATT regimen and 8 weeks of high-dose aspirin or placebo. The primary outcome for the first randomisation is all-cause mortality, and for the second randomisation is the paediatric modified Rankin Scale (mRS), both at 48 weeks. Nested substudies include pharmacokinetics, pharmacogenetics, pathophysiology, diagnostics and prognostic biomarkers, in-depth neurodevelopmental outcomes, MRI and health economics.

ETHICS AND DISSEMINATION: Local ethics committees at all participating study sites and respective regulators approved the SURE protocol. Ethics approval was also obtained from UCL, UK (14935/001). Informed consent from parents/carers and assent from age-appropriate children are required for all participants. Results will be published in international peer-reviewed journals, and appropriate media will be used to summarise results for patients and their families and policymakers.

TRIAL REGISTRATION: ISRCTN40829906 (registered 13 November 2018).


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