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A Retrospective Study of Treatment Patterns and Clinical Outcomes in Patients With Central Nervous System Tuberculosis

A Retrospective Study of Treatment Patterns and Clinical Outcomes in Patients With Central Nervous System Tuberculosis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06011915
Enrollment
638
Registered
2023-08-25
Start date
2017-08-22
Completion date
2023-07-26
Last updated
2023-08-28

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

Conditions

Central Nervous System Tuberculosis

Brief summary

This is a retrospective clinical study to analyze the clinical characteristics, complications, and effects of different treatment options on long-term prognosis in patients with central nervous system tuberculosis. All cases of central nervous system tuberculosis diagnosed between 2016 and 2021 were included in the electronic medical record system of one center, and data such as demographics, hospitalization information, clinical information, laboratory or imaging examinations, treatment plans, and outcomes were collected.

Interventions

None listed

Sponsors

Tongji Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* The patient meets the following criteria 1) or 2) or 3): 1. The discharge diagnosis is central nervous system tuberculosis, refer to the ICD-10 code related to central nervous system tuberculosis. 2. The discharge diagnosis was tuberculous meningitis (ICD-10: A17.000), or tuberculous cerebrospinal meningitis (ICD-10: A17.001), or tuberculous meningoencephalitis (ICD-10: A17.803 ), or tuberculous encephalitis (ICD-10: A17.804), or tuberculous brain abscess (ICD-10: A17.805), or spinal tuberculosis (ICD-10: A17.806), or tuberculous encephalitis Water (ICD-10: A17.807). 3. Tuberculous meningitis diagnosed according to the Guidelines for Diagnosis and Treatment of Central Nervous System Tuberculosis in China (2019 Edition) * Age and gender are not limited.

Exclusion criteria

* Patients with no clear diagnosis at discharge. * Patients judged by the investigator to be unsuitable for inclusion in this protocol.

Design outcomes

Primary

MeasureTime frameDescription
2-year survival rate1 years,2 yearsCalculate the 1-year survival rate and 2-year survival rate.
2-year disability rate1 years,2 yearsCalculate the 1-year disability rate and 2-year disability rate. Common disabilities include aphasia, hemiplegia, paraplegia, deafness, blindness, mental retardation, etc. For reference, please refer to the 《Grading of Human Injury and Disability Degree》 and 《Guidance for determination of cause-and-effect relationship between personal injury and disease》.

Secondary

MeasureTime frameDescription
Incidence of complications in patients with different treatment regimens2 yearsThe electronic medical record system was used to collect patients' complications from baseline (admission) to 24 months, and the incidence of complications of different treatment options was compared.
Clinical features: age of onset, mode of onset2 yearsage of onset, mode of onset
proportion of patients admitted to ICU2 years
length of hospital stay2 years
The presense of clinical symptoms of patients2 yearsThe number and severity of clinical symptoms of patients.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026