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Clinical Trial Summary

The objective of the study is to evaluate the efficacy of Polymyxin B for treatment Gram negative bacterial infection. The hypothesis of study is Polymyxin B would be the new antibacterial agents for Thai Gram negative infected patients in case of desirable outcomes and minimal side effects.


Clinical Trial Description

- Investigator is notified by doctors who take care of gram negative infected patients.

- Investigator inform patient or their relatives about all topics in project, eligible criteria, method, material and monitoring treatment.

- After patient or their relatives are appreciated to join this project, investigator collect data in case record form;electronics form, then implement the drug.

- Duration of treatment is determined by site and severity of infection, approximately 7-14 days.

- Sample size calculation, by prevalence formula, we estimate the mortality rate about 50 %, deviation 10 %,and 2-sided 95% Confidence interval, therefore,97 persons

- We estimate gather data about 100 persons.

- Statistical descriptive analysis for descriptive data.

- During the study is performing, all unexpected adverse event definitely report to Siriraj institutional Review Board immediately, in addition to subjects or their relatives. ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02328183
Study type Interventional
Source Mahidol University
Contact Thundon Ngamprasertchai, MD.
Phone 66850887736
Email thundon_ngamprasertchai@hotmail.com
Status Recruiting
Phase Phase 4
Start date December 2014
Completion date November 2015

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