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Clinical Trial Summary

The principal objective is to evaluate a cure rate and number of adverse events of with confirmed multidrug-resistant tuberculosis patient treated with a 9months regimen.


Clinical Trial Description

Study participants will be followed up, under existing protocol derived from a study protocol developed by the "Union internationale contre les maladies respiratoires" and carried out already in 9 Africans countries. Participants will be hospitalised for at least four month, period which they will be given treatments, assessed for adverse events, monitored for TB-MR strains using culture techniques, at the monthly basis. If patients found with negative sputum culture at month four they will be dischrged from the hospital, and then treated four an additional five montns and then follow up, clinically and biologically for an additional six months before being declared as cured. ;


Study Design


Related Conditions & MeSH terms

  • Multi-drug Resistant Tuberculosis
  • Tuberculosis
  • Tuberculosis, Multidrug-Resistant

NCT number NCT03057756
Study type Observational [Patient Registry]
Source Centre de Recherche Médicale de Lambaréné
Contact Ayola A Adegnika, MD, PhD
Phone +24107406464
Email aadegnika@cermel.org
Status Recruiting
Phase
Start date September 11, 2015
Completion date July 1, 2023

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