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Recruiting NCT07929519

NCT07929519 Clinical Characteristics, Treatment, Diagnostic Findings, and Outcomes of Tuberculous Meningitis in Indonesia, 2022-2025

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Clinical Trial Summary
NCT ID NCT07929519
Status Recruiting
Phase —
Sponsor Ina-Respond
Condition Tuberculous Meningitis
Study Type OBSERVATIONAL
Enrollment 300 participants
Start Date 2026-09-24
Primary Completion 2027-08-31

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
No intervention (observational study)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 300 participants in total. It began in 2026-09-24 with a primary completion date of 2027-08-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

TBM Study is a multicenter, observational, retrospective cohort study of Tuberculous Meningitis (TBM) patients who underwent treatment at the hospital during the 2022-2025 period. The goal of this study is to learn about the clinical characteristics, diagnostic findings, drug resistance profiles, treatment regimens, complications, and treatment outcomes of patients diagnosed with TBM who were admitted to the study hospitals between 2022 and 2025. This study uses retrospective data obtained from electronic medical records (EMR).

Eligibility Criteria

Inclusion Criteria: * Admited to the participating hospital sites between January 1, 2022, and December 31, 2025 * Have a discharge diagnosis of TBM (ICD-10 code A17.0) or documented TBM diagnosis in the hospital EMR system. * Have accessible data available in the EMR. Exclusion Criteria: None

Contact & Investigator

Central Contact

dr. M. Helmi Aziz, M.Sc., Sp.MK

✉ mhazis@ina-respond.net

📞 +62 858-5458-0905

Principal Investigator

dr. Robert Sinto, SpPD,, K-PTI, DPhil, FINASIM, FHEA

PRINCIPAL INVESTIGATOR

Indonesia Research Partnership on Infectious Disease (INA-RESPOND)

Frequently Asked Questions

Who can join the NCT07929519 clinical trial?

This trial is open to participants of all sexes, studying Tuberculous Meningitis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07929519 currently recruiting?

Yes, NCT07929519 is actively recruiting participants. Contact the research team at mhazis@ina-respond.net for enrollment information.

Where is the NCT07929519 trial being conducted?

This trial is being conducted at Denpasar, Indonesia, Jakarta, Indonesia, Jakarta, Indonesia, Ambon City, Indonesia and 2 additional locations.

Who is sponsoring the NCT07929519 clinical trial?

NCT07929519 is sponsored by Ina-Respond. The principal investigator is dr. Robert Sinto, SpPD,, K-PTI, DPhil, FINASIM, FHEA at Indonesia Research Partnership on Infectious Disease (INA-RESPOND). The trial plans to enroll 300 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology