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Last Updated: November 16, 2024

CLINICAL TRIALS PROFILE FOR MAXIPIME


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All Clinical Trials for MAXIPIME

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00609375 ↗ Efficacy of Cefepime Continuous Infusion Versus an Intermittent Dosing Regimen Completed Asociacion Colombiana de Infectologia, ACIN. Infectious Diseases Society of Colombia Phase 4 2006-09-01 To determine the efficacy of the administration of 7 to 14 days of cefepime in a continuous infusion vs an intermittent (every 8 hours) administration, in adult patients hospitalized in Bogotá with sepsis and bacteremia caused by gram negative bacilli. The outcome was the rate of clinical cure and microbiological cure after 7 and 14 days of initiation of therapy and rates of relapse after 28 days. Hypothesis: The administration of beta lactams in continuous infusion allows a clinical or microbiological cure greater than the intermittent administration.
NCT00609375 ↗ Efficacy of Cefepime Continuous Infusion Versus an Intermittent Dosing Regimen Completed Clinica Palermo, Bogota Phase 4 2006-09-01 To determine the efficacy of the administration of 7 to 14 days of cefepime in a continuous infusion vs an intermittent (every 8 hours) administration, in adult patients hospitalized in Bogotá with sepsis and bacteremia caused by gram negative bacilli. The outcome was the rate of clinical cure and microbiological cure after 7 and 14 days of initiation of therapy and rates of relapse after 28 days. Hypothesis: The administration of beta lactams in continuous infusion allows a clinical or microbiological cure greater than the intermittent administration.
NCT00609375 ↗ Efficacy of Cefepime Continuous Infusion Versus an Intermittent Dosing Regimen Completed Fundación San Carlos, Bogota Phase 4 2006-09-01 To determine the efficacy of the administration of 7 to 14 days of cefepime in a continuous infusion vs an intermittent (every 8 hours) administration, in adult patients hospitalized in Bogotá with sepsis and bacteremia caused by gram negative bacilli. The outcome was the rate of clinical cure and microbiological cure after 7 and 14 days of initiation of therapy and rates of relapse after 28 days. Hypothesis: The administration of beta lactams in continuous infusion allows a clinical or microbiological cure greater than the intermittent administration.
NCT00609375 ↗ Efficacy of Cefepime Continuous Infusion Versus an Intermittent Dosing Regimen Completed Hospital san Jorge, Pereira Phase 4 2006-09-01 To determine the efficacy of the administration of 7 to 14 days of cefepime in a continuous infusion vs an intermittent (every 8 hours) administration, in adult patients hospitalized in Bogotá with sepsis and bacteremia caused by gram negative bacilli. The outcome was the rate of clinical cure and microbiological cure after 7 and 14 days of initiation of therapy and rates of relapse after 28 days. Hypothesis: The administration of beta lactams in continuous infusion allows a clinical or microbiological cure greater than the intermittent administration.
NCT00609375 ↗ Efficacy of Cefepime Continuous Infusion Versus an Intermittent Dosing Regimen Completed Hospital san Juan de Dios, Antioquia Phase 4 2006-09-01 To determine the efficacy of the administration of 7 to 14 days of cefepime in a continuous infusion vs an intermittent (every 8 hours) administration, in adult patients hospitalized in Bogotá with sepsis and bacteremia caused by gram negative bacilli. The outcome was the rate of clinical cure and microbiological cure after 7 and 14 days of initiation of therapy and rates of relapse after 28 days. Hypothesis: The administration of beta lactams in continuous infusion allows a clinical or microbiological cure greater than the intermittent administration.
NCT00609375 ↗ Efficacy of Cefepime Continuous Infusion Versus an Intermittent Dosing Regimen Completed Hospital Santa Clara, Bogota Phase 4 2006-09-01 To determine the efficacy of the administration of 7 to 14 days of cefepime in a continuous infusion vs an intermittent (every 8 hours) administration, in adult patients hospitalized in Bogotá with sepsis and bacteremia caused by gram negative bacilli. The outcome was the rate of clinical cure and microbiological cure after 7 and 14 days of initiation of therapy and rates of relapse after 28 days. Hypothesis: The administration of beta lactams in continuous infusion allows a clinical or microbiological cure greater than the intermittent administration.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for MAXIPIME

Condition Name

Condition Name for MAXIPIME
Intervention Trials
Pseudomonas Aeruginosa 1
Breast Cancer 1
Grade 1 Follicular Lymphoma 1
Neoplasms 1
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Condition MeSH

Condition MeSH for MAXIPIME
Intervention Trials
Communicable Diseases 2
Febrile Neutropenia 2
Urinary Tract Infections 2
Infections 2
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Clinical Trial Locations for MAXIPIME

Trials by Country

Trials by Country for MAXIPIME
Location Trials
Colombia 3
Russian Federation 2
United States 2
Egypt 1
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Trials by US State

Trials by US State for MAXIPIME
Location Trials
Texas 1
North Carolina 1
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Clinical Trial Progress for MAXIPIME

Clinical Trial Phase

Clinical Trial Phase for MAXIPIME
Clinical Trial Phase Trials
Phase 4 1
Phase 3 1
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for MAXIPIME
Clinical Trial Phase Trials
Terminated 2
Completed 2
Recruiting 1
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Clinical Trial Sponsors for MAXIPIME

Sponsor Name

Sponsor Name for MAXIPIME
Sponsor Trials
Forest Laboratories 1
Clinica Palermo, Bogota 1
Accellena Research and Development 1
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Sponsor Type

Sponsor Type for MAXIPIME
Sponsor Trials
Other 14
Industry 2
NIH 1
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