RecruitingPhase 2NCT06446245

Adjunctive Doxycycline for Central Nervous System Tuberculosis

DIRECT: Doxycycline Adjunctive Therapy to Reduce Excess Mortality and Complications From Central Nervous System Tuberculosis - Phase II Randomized Clinical Trial


Sponsor

National University Hospital, Singapore

Enrollment

200 participants

Start Date

Aug 21, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Although tuberculosis is now considered a treatable disease, central nervous system tuberculosis (CNS-TB) when managed with the current standard-of-care (SOC), still has mortality rates ranging from 30-50% even in tertiary hospital centers. At present, the SOC for the management of CNS-TB is anti-tuberculous therapy with adjunctive corticosteroids. In CNS-TB, the activity of pathogenic host matrix metalloproteinases (MMPs) is unopposed to tissue inhibitors of metalloproteinases (TIMPs), resulting in a matrix-degrading phenotype which may drive worse outcomes in CNS-TB. In a prior established CNS-TB murine model, the investigators have demonstrated that adjunctive MMP inhibition using doxycycline, a widely available and cheap drug, in addition to standard TB treatment, compared with standard TB treatment alone, improved murine survival (Manuscript in preparation). The investigators previously showed that in humans with pulmonary TB, doxycycline with anti-TB treatment is safe, accelerates the resolution of inflammation, and suppresses systemic and respiratory MMPs. Hence, the investigators are now ideally positioned to determine if adjunctive doxycycline in patients with CNS-TB can improve clinical outcomes. The investigators will perform a Phase 2 double-blind randomized-controlled trial (RCT) of adjunctive doxycycline versus placebo with standard TB treatment and steroids for 8 weeks, with the primary outcome of 8-week mortality or severe neurological deficits.


Eligibility

Min Age: 21 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Adjunctive corticosteroid, Anti Tuberculosis Drug, and others for people with tuberculosis, central nervous system, tuberculosis, meningeal, and other related conditions. The study is currently recruiting participants at 6 locations. People eligible for this study include aged 21 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGDoxycycline

adjunctive doxycycline to standard anti-tuberculous treatment and corticosteroid therapy

DRUGPlacebo

Placebo

DRUGAnti Tuberculosis Drug

Standard anti-tuberculous therapy

DRUGAdjunctive corticosteroid

Adjunctive corticosteroids to be dosed at 0.4mg/kg/day of dexamethasone or equivalent for week 1, then 0.3mg/kg/day for week 2, 0.2mg/kg/day for week 3, 0.1mg/kg/day for week 4, then tapered to stop over the next 4 weeks. Other forms of corticosteroids are also acceptable eg. hydrocortisone, methylprednisolone at the equivalent dosage


Locations(6)

Adam Malik Hospital

Medan, Medan, Indonesia

Universitas Sumatera Utara

Medan, Medan, Indonesia

Murni Teguh Memorial Hospital

Medan, Indonesia

Sarawak General Hospital

Kuching, Sarawak, Malaysia

National University Hospital

Singapore, Singapore, Singapore

Tan Tock Seng Hospital

Singapore, Singapore

View Full Details on ClinicalTrials.gov

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NCT06446245