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Retrospective Real-word Study of Linezolid for the Treatment of Tuberculous Meningitis

Retrospective Real-word Study of Linezolid for the Treatment of Tuberculous Meningitis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03898635
Enrollment
150
Registered
2019-04-02
Start date
2018-01-01
Completion date
2019-06-01
Last updated
2019-04-02

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

Conditions

Tuberculous Meningitis

Keywords

linezolid

Brief summary

Tuberculous meningitis (TBM) is the most serious form of Mycobacterium tuberculosis infection, causing mortality and disability in more than half of the patients. Current standard treatment for TBM is based on those developed to treat pulmonary tuberculosis, which does not take into account the differential ability of anti-tuberculosis drugs to penetrate the brain. With both good central nervous system penetrance and anti-tuberculosis efficacy that have been demonstrated in drug-resistant tuberculosis, linezolid may be a promising antimicrobial in TBM treatment. The purpose of this study is to evaluate the effectiveness of linezolid in the treatment of TBM.

Interventions

DRUGLinezolid

To add linezolid 600mg or 1200mg daily in the initial or subsequent treatment regimen of TBM.

Sponsors

Huashan Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* all patients diagnosed as TBM from the electronic medical record system.

Exclusion criteria

* Does not meet the established diagnostic criteria; * Combine other pathogen central infections; * Follow-up confirmed that the final diagnosis considers other diseases (such as tumors, autoimmune encephalitis, etc.); * Our hospital has less than one week of anti-tuberculosis treatment; * Lack of information

Design outcomes

Primary

MeasureTime frame
Survival5 years

Secondary

MeasureTime frame
Number of participants with Medical Research Council grade deteriorationFrom the beginning of anti-tuberculosis treatment to the first documented progression, assessed up to 5 years.

Other

MeasureTime frameDescription
Time of Glasgow Coma Scale recovered to 15From the beginning of anti-tuberculosis treatment to the first documented recovery, assessed up to 5 years.
Time of body temperature returns to normalFrom the beginning of anti-tuberculosis treatment to the first documented recovery, assessed up to 5 years.
Number of participants with new omplicationsFrom the beginning of anti-tuberculosis treatment to the first documented progression, assessed up to 5 years.Hydrocephalus, cerebral infarction, epilepsy, brain abscess, tuberculoma

Countries

China

Contacts

Primary ContactXian Zhou
zhouxian-13@163.com(86)18801734036
Backup ContactFeng Sun
aaronsf1125@126.com

Outcome results

None listed

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