Skip to main content
OpenTrials
Completed

NCT Number: NCT01158755

Intensified Treatment Regimens for TB Meningitis: PK, PD and Tolerability Study

Tuberculous meningitis (TBM) is the most lethal form of tuberculosis infection, and is diagnosed in approximately 5-10% of TB patients. The incidence of TBM has increased considerably during the last decade, partly due to the HIV epidemic. Without treatment, virtually all patients with TB meningitis will die. With the current treatment regimens, TBM is fatal in approximately 30-50% of cases, and responsible for severe disability in a similar proportion of survivors.

Worldwide, Indonesia the third highest case load of tuberculosis with an estimated 500,000 new patients / year. Representative data are lacking, but it is clear that TBM is a growing problem. For instance, in Hasan Sadikin Hospital, the top-referral hospital for West Java Province (population 40 million), Indonesia, 40-50 cases of TBM were treated yearly in the late 90's compared to approximately 100 in recent years.

There is very little evidence for the current treatment regimen for TBM, which dates back to the late 60's. Therefore, there is an urgent need to evaluate intensified treatment of TBM in randomized trials. We hypothesize that higher dose rifampicin, moxifloxacin (possibly also at high dose), or both will improve outcome of TBM. To determine the experimental regimen(s) which should be compared with current regimen in phase 3 trials, we want to evaluate pharmacokinetic aspects and toxicity of candidate regimens in a phase 2 clinical trial in 60 patients with TBM in Indonesia.

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Tuberculous meningitis, diagnosed based on clinical and/or CSF criteria
  • Age 15 years old or more
  • Hospitalized for the treatment

Exclusion criteria

  • Pregnancy/lactation
  • On TB treatment within 7 days before inclusion
  • Elevated liver enzyme (> 5x than normal values)
  • Known hypersensitivity/intolerance to rifampicin or moxifloxacin
  • Prolonged QTc interval in ECG or other detectable cardiac arrythmias, in the absence of hypokalemia
  • Refusal to be included in the study

Treatment and study plan

moxifloxacin

Drug

Subjects on both arms will further be randomized into receiving moxifloxacin either in standard dose (400 mg p.o.), high dose (800 mg p.o.) of moxifloxacin, or not receiving moxifloxacin (ethambutol 750 mg p.o., instead) Intervention drug will be given for 14 days, and the drug will be switched to ethambutol 750 mg p.o. (in accordance with National TB Program)

Other names: Avelox (r)

Primary outcomes

  1. Rifampicin and Moxifloxacin concentration in plasma and CSF

    Time frame: Plasma drug concentration samplings at 0, 1, 2, 4, 6 and 24h post dose (6 time points). CSF samples at 2 time points.

    On sampling day (one of the first 3 days of hospitalization), we will measure plasma and CSF drug concentration at several time points.

    Plasma drug concentration will be measured at 6 time points (hour 0, 1, 2, 4, 6 and 12).

    CSF drug concentration at 2 time points: (1) hour 3-6 post dose on the same blood sampling day and (2) within 5 days after the 1st day of TB drug administration, 1-3 hours after drug intake

Secondary outcomes

  1. Early and late mortality

    Time frame: 1st and 6th month of TB treatment

    We will measure early (within first month of TB treatment) and late (after 6 months of TB treatment) mortality

Sponsors and collaborators

Lead sponsor

Universitas Padjadjaran

Other

Collaborators

  • Radboud University Medical Center

Registry information

Official study title

Comparison of Intensive Treatment Regimens and Standard Treatment Regimen for Tuberculous Meningitis: Pharmacokinetics, Pharmacodynamics and Tolerability Study

Important dates

Study start
2010
Primary completion
2011
Study completion
2012
First posted
Jul 8, 2010
Registry last updated
Jun 7, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.