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Prospective cohort study of immunomodulatory therapy for tuberculous meningitis based on LTA4H gene polymorphism

Basic and clinical cohort study for immunomodulatory therapy in tuberculous meningitis patients from Xizang based on LTA4H gene polymorphism

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096085
Enrollment
Unknown
Registered
2025-01-17
Start date
2025-01-30
Completion date
Unknown
Last updated
2025-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tuberculous meningitis

Interventions

anti-tuberculosis treatment group:Patients were divided into three groups. This group is the standard anti-tuberculosis treatment group.
dexamethasone group:The patients were divided into three groups. The group was anti-tuberculosis + dexamethasone treatment group.
thalidomide group:The patients were divided into three groups. The group was anti-tuberculosis + thalidomide treatment group.

Sponsors

Department of Infectious Diseases, General Hospital of Xizang Military Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Participants must be aged between 18 and 65 years, regardless of gender; 2. Clinical symptoms and/or imaging (head MRI or CT) support the diagnosis of tuberculous meningitis; 3. No drug-resistance during initial tuberculosis treatment; 4. No previous treatment with hormones, immunosuppressants or biological agents; 5. Voluntarily sign the informed consent to participate in the project, and be able and willing to accept follow-up visits

Exclusion criteria

Exclusion criteria: 1. Participants with plans for pregnancy or currently pregnant, regardless of gender; 2. Lactating women; 3. Allergic to thalidomide; 4. Intolerant to thalidomide/first-line anti-tuberculosis drug therapy (isoniazid + rifampicin + ethambutol + pyrazinamide) or appearing severe drug reactions; 5. Participants with severe infections, autoimmune diseases, severe liver or kidney insufficiency, blood or tumor disorders; 6. Any other significant medical conditions, laboratory abnormalities or mental illnesses that the researcher considers inappropriate for inclusion.

Design outcomes

Primary

MeasureTime frame
TNFa;LTB4;

Secondary

MeasureTime frame
LTA4H mRNA;Modified Rankin Scale;Glasgow Coma Scale;TNFa mRNA;

Countries

China

Contacts

Public ContactQianqi Wei

General Hospital of Xizang Military Command

infection0522@163.com+86 185 0599 3553

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026