Fluconazole Versus Micafungin for Candida Bloodstream Infection in Non-Neutropenic Patients

This study has been withdrawn prior to enrollment.
(Subjects were not recruited as intended.)
Sponsor:
Collaborators:
Pfizer
Astellas Pharma Inc
Information provided by:
Kyoto University
ClinicalTrials.gov Identifier:
NCT00304772
First received: March 17, 2006
Last updated: March 24, 2009
Last verified: March 2009

March 17, 2006
March 24, 2009
August 2006
December 2008   (final data collection date for primary outcome measure)
Treatment success (completion of protocol treatment within 12 weeks and recurrence-free survival at 4 weeks after the completion of protocol treatment) [ Time Frame: 12 weeks and 4 weeks ] [ Designated as safety issue: No ]
Treatment success (completion of protocol treatment within 12 weeks and recurrence-free survival at 4 weeks after the completion of protocol treatment)
Complete list of historical versions of study NCT00304772 on ClinicalTrials.gov Archive Site
  • Safety [ Time Frame: 12 weeks and 4 weeks ] [ Designated as safety issue: Yes ]
  • Duration of protocol treatment period in patients with treatment success [ Time Frame: 12 weeks and 4 weeks ] [ Designated as safety issue: No ]
  • Overall survival at 4 and 12 weeks [ Time Frame: 12 weeks and 4 weeks ] [ Designated as safety issue: No ]
  • Recurrence in patients who completed protocol treatment [ Time Frame: 12 weeks and 4 weeks ] [ Designated as safety issue: No ]
  • Occurrence and deterioration of endophthalmitis during protocol treatment [ Time Frame: 12 weeks and 4 weeks ] [ Designated as safety issue: No ]
  • Treatment success according to causative species, antifungal susceptibility profile, underlying condition [ Time Frame: 12 weeks and 4 weeks ] [ Designated as safety issue: No ]
  • Safety
  • Duration of protocol treatment period in patients with treatment success
  • Overall survival at 4 and 12 weeks
  • Recurrence in patients who completed protocol treatment
  • Occurrence and deterioration of endophthalmitis during protocol treatment
  • Treatment success according to causative species, antifungal susceptibility profile, underlying condition
Not Provided
Not Provided
 
Fluconazole Versus Micafungin for Candida Bloodstream Infection in Non-Neutropenic Patients
A Randomized Comparative Study of Fluconazole Versus Micafungin for the Treatment of Candida Bloodstream Infection in Non-Neutropenic Patients

The purpose of this study is to verify the equivalence in clinical efficacy of fluconazole and micafungin for the treatment of Candida bloodstream infection in non-neutropenic patients.

Candida bloodstream infection occurs in patients with poor general conditions and has poor prognosis with attributable mortality of more than 30%. Clinical efficacy of fluconazole for the treatment of Candida bloodstream infection has been reported in clinical studies, since 1985 when it placed on the market. Fluconazole has established a position as the first-line drug up to date. However, possibly associated with the increased use of fluconazole, increased frequency of Candida species or strains with low susceptibility to fluconazole has been pointed out. Micafungin, an antifungal echinocandin with a different antifungal mechanism from fluconazole, has been reported to show good in vitro activity to various Candida species and strains with fluconazole resistance, and has comparative clinical efficacy with fluconazole for esophageal candidiasis, while it has relatively low in vitro activity to certain Candida species. There is no comparative study of fluconazole versus micafungin against Candida bloodstream infection.

Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
  • Candidiasis
  • Sepsis
  • Drug: Fluconazole
    400mg/day
  • Drug: Micafungin
    150mg/day
  • Active Comparator: 1
    Intervention: Drug: Fluconazole
  • Active Comparator: 2
    Intervention: Drug: Micafungin
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
190
December 2008
December 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients in whom Candida species have been isolated from blood culture.
  • Patients accompanied by systemic infectious symptoms during the period from 24 hours (h) before collection of blood culture showing a positive result.
  • Patients aged 20 years or older on the date of registration.
  • Patients who have not received systemic administration of antifungal agents or who have started such administration within 48 h.
  • Patients in whom a central venous (CV) catheter has been removed during the period from 24 h before collection of blood culture showing a positive result to registration, or a CV catheter can be removed within 72 h after registration.
  • Patients with no verified undrainable abscess with a diameter of at least 3 cm, or impassable occlusive lesions, which are possibly attributable to Candida species.
  • Patients from whom written informed consent to participate in this study has been obtained (or from their legally acceptable representatives).
  • Patients who have adequate neutrophil count and hepatic/renal function in the blood test performed within 72 h before registration.

Exclusion Criteria:

  • Patients with a history of adverse reactions associated with fluconazole or micafungin.
  • Patients who have been treated with fluconazole or micafungin for at least 1 week within 12 weeks.
  • Patients with a history of detection of fluconazole non-susceptible Candida species within 12 weeks.
  • Patients in whom the neutrophil count is predicted to decrease to below 500/mL.
  • Patients who are not treated with terfenadine, triazolam, cisapride, and ergotamine, which are contraindicated for concomitant use with fluconazole.
  • Patients who are determined to be ineligible by the investigator.
Both
Not Provided
No
Contact information is only displayed when the study is recruiting subjects
Japan
 
NCT00304772
JCRID0502
No
Shunji Takakura, Kyoto University Hospital
Kyoto University
  • Pfizer
  • Astellas Pharma Inc
Study Chair: Satoshi Ichiyama, MD, PhD Professor of Medicine, Department of Clinical Laboratory Medicine, Kyoto University Hospital
Principal Investigator: Shunji Takakura, MD, PhD Instructor in Medicine, Department of Clinical Laboratory Medicine, Kyoto University Hospital
Kyoto University
March 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP