Multicentric Study About the Usefulness of Monitoring Plasma Levels of Colistin and Sodium Colistimethate in Patients With Infections Due to Multi-drug Resistant Gram Negative Bacilli, Treated With Colistin

NCT ID: NCT01845246

Last Updated: 2017-04-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 101 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-01-31
• Study Completion Date: 2015-08-31

Brief Summary

Objectives: Main objective: to assess the impact of an intervention for optimizing the dosing of colistin based on its plasma levels in patients with infections due to multi-drug resistant gram negative bacilli. The impact will be evaluated in terms of clinical and microbiological outcome, and toxicity.

Secondary objectives:

1. To determine the percentage of patients reaching plasma levels considered adequate (Cmax / MIC 8-10) for the treatment of infections due to gram-negative bacilli susceptible to colistin, in the cohort of patients treated with standard doses of this drug without adjusting the dose.

2. To analyze the possible emergence of bacterial resistance to this drug and its relationship to the calculated colistin pharmacokinetic and pharmacodynamic indexes.

Methods:

Design: open controlled trial, blinded for the analyst, to be performed at thre tertiary care Hospitals in Barcelona.

Subjects: Patients attended consecutively between 2012 and 2013 infected with multi-drug resistant gram negative bacilli and treated with colistin.

Sample size: 142 cases. Intervention: Once detected the infection requiring treatment with colistin, patients will be randomized to receive the intervention or not, with a 1:1 ratio. The intervention will be performed by an Infectious Diseases physician and will consist in a recommendation on the dose of colistin based on its plasma levels 48 hours after treatment onset.

Variables: peak and through colistin levels 48 hours after treatment onset, clinical, analytical and microbiological data at baseline and during follow-up of the patients.

Outcome measures: clinical, microbiological and toxicity data. Analysis: Comparison of patient characteristics and outcome variables between patients who had received the intervention and those who had not. The analysis will be done by intention to treat, by biological effectiveness and by compliance with the protocol.

Conditions

Multidrug Resistant Gram Negative Bacterial Infections

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Standard doses of colistin will be used.

Patients will receive the standard doses of colistin without TDM (Therapeutic drug monitoring).

Group Type: NO_INTERVENTION

No interventions assigned to this group

Prospective TDM (Therapeutic drug monitoring)of colistin arm

CMS dose will be adjusted based on protocol obtained TDM levels.

Group Type: EXPERIMENTAL

Prospective TDM Arm of colistin

Intervention Type: DEVICE

Interventions

Prospective TDM Arm of colistin

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Male or female ≥18 years of age.
• Hospitalized patients with an active infection caused by MDR-BGN
• Treatment with intravenous CMS for at least 3 consecutive days
• Evidence of a personally signed and dated informed consent document in accordance with local regulatory and legal requirements indicating that the subject (or a legally acceptable representative) has been informed of all pertinent aspects of the study.

Exclusion Criteria

• Patients colonized by a MDR-BGN and no signs/symptoms of an active infection
• Treatment with intravenous CMS for least than 3 days
• Patients with polymicrobial infections (with an isolated microorganism different from the MDR-BGN).
• Patients with a glomerular filtration rate at baseline less than 10ml/min or those requiring renal replacement therapies.
• Known history of allergy, hypersensitivity or serious reaction to polymyxins.
• Patients treated with nebulized CMS in addition to intravenous CMS.
• Patients who have already participated in this trial.
• Patients without a personally signed and dated informed consent document

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Parc de Salut Mar

OTHER

Sponsor Role: lead

Responsible Party

Juan Pablo Horcajada

MD

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Hospital del Mar

Barcelona, Barcelona, Spain

Hospital de Sant Pau

Barcelona, Barcelona, Spain

Hospital de Granollers

Granollers, Barcelona, Spain

Countries

Spain

Other Identifiers

PSM-COL-MC-12

Identifier Type: -

Identifier Source: org_study_id