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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00386802
Other study ID # 2005-004973-55
Secondary ID ANTIVORIFUNGOL
Status Completed
Phase Phase 4
First received October 11, 2006
Last updated September 17, 2009
Start date August 2006
Est. completion date January 2009

Study information

Verified date September 2009
Source PETHEMA Foundation
Contact n/a
Is FDA regulated No
Health authority Spain: Ministry of Health
Study type Interventional

Clinical Trial Summary

Primary purpose: Frequency of use of broad-spectrum antifungals in the episode of neutropenia.

Secondary purposes:To determine the safety and toxicity measure by:

1. Frequency of Invader Fungal Infection.

2. Frequency of global use of broad-spectrum antifungals as amphotericine, itraconazole, voriconazole, caspofungin, terbinafine, during the period of study.

3. Mortality

4. Development of nephrotoxicity

5. Use of galactomannan in this clinical context

6. Time of administration of empirical antifungal therapy of broad-spectrum.


Description:

Clinical trial with a pharmaceutical speciality in the conditions of authorized use


Recruitment information / eligibility

Status Completed
Enrollment 115
Est. completion date January 2009
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group 2 Years and older
Eligibility Inclusion Criteria:

- Adult and pediatric patients (from 2 years old on) with diagnostic of hematologic malignancies or solid tumour.

- Patients who will develop neutropenia (<500PN) post chemotherapy or post Bone Marrow Transplantation (BMT) that according to the center, they can receive empirical antifungal treatment of broad-spectrum.

- Controlled patients with galactomannan in blood twice weekly.

- Empirical antibacterial therapy of broad-spectrum, as possible the Pethema protocol that it is activated in this moment. Also it will be validated the monotherapy with carbapenemic or cephalosporin of fourth or third generation, or the biotherapy.

- Inclusion of patient since the start of his chemotherapy or therapy of preparation.

- If a bacterial infection is documented, it will be treated and controlled before to begin the empirical antifungal treatment.

- Signed of informed consent.

- Negative pregnancy test in fertile patients

Exclusion Criteria:

- Use of antifungal prophylaxis with triazoles with activity against Aspergillus, or use of others systematics antifungal by previous Invader Fungal Infection or other reasons.

- Use prophylactic of fluconazole to dose higher than 100 mg/day.

- Allergy to azoles

- To have a invader fungal infection at start of episode of neutropenia with fever.

- High effect in the unity of insulation of Candida strong to fluconazole that to opinion of center it hasn´t appropriate to include in a protocol where it is considered the use of empirical fluconazole.

- Neutropenias made by aplastic anemia or other faults of bone similar.

- Inclusion previous in this study.

- The patients will be excluded if they have settled by Aspergillus, C.krusei or C.gladiata in this episode of neutropenia, or in other and if they lack of the results of the cultures of vigilance in the present episode. If it presents positive result for any of those pathogens the empirical treatment will must be with a antifungal that it covers good (amphotericin, caspofungin or voriconazole) and not with fluconazole, then those patients will not follow this protocol.

- To receive drugs, which aren´t indicated in patients in treatment with voriconazole and/or with fluconazole.

- The patients will not be excluded if they receive antibacterial prophylaxis oral with quinolones, macrolides, etc., or stimulating factors G-CSF, GM-CSF or similar.

- Cause of exclusion will be the fault of fulfilment of inclusion criteria. Above all the patients will be excluded if they:

- have fault of twice weekly monitoring with galactomannan.

- have a bacterial infection not very good treated and controlled before to can begin the empirical antifungal infection (according to definition previous)

- have at final, a neutropenia of short stay that it has a risk important of Invader Fungal Infection. This data naturally will not know in the moment of include at patient in the study. It defines as neutropenia of short stay if it last out less of 5 days.

Study Design

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


Related Conditions & MeSH terms


Intervention

Drug:
Antifungal drug. VORICONAZOL. (VFEND®)
I.V charge dose 6 mg/kg/12h (2 doses) Maintenance iv treatment 4 mg/kg/12h during 6 days, followed by oral treatment (200 mg/12h)

Locations

Country Name City State
Spain Hospital Clínic Barcelona
Spain Hospital Virgen de las Nieves Granada
Spain Hospital General de Jerez de la Frontera Jerez de la Frontera Cádiz
Spain Hospital General Universitario Gregorio Marañón, Madrid Madrid
Spain Hospital Universitario de la Princesa Madrid
Spain Hospital Universitario Ramón y Cajal, Madrid Madrid
Spain Hospital Universitario Morales Meseguer, Murcia Murcia
Spain Hospital Son Llatzer Palma de Mallorca Mallorca
Spain Hospital Clínico Universitario de Salamanca Salamanca
Spain Hospital Universitario Marqués de Valdecilla Santander
Spain Hospital Clínico Universitario de Valencia Valencia
Spain Hospital Universitario La Fe Valencia
Spain Hospital Clínico Lozano Blesa Zaragoza

Sponsors (1)

Lead Sponsor Collaborator
PETHEMA Foundation

Country where clinical trial is conducted

Spain, 

References & Publications (37)

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* Note: There are 37 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary Frequency of use of broad-spectrum antifungals in the episode of neutropenia. 2 years No
Secondary To determine the safety and toxicity measure by: 1 year Yes
Secondary Frequency of Invader Fungal Infection. 2 years No
Secondary Frequency of global use of broad-spectrum antifungals as amphotericine, itraconazole, voriconazole, caspofungin, terbinafine, during the period of study. 2 years No
Secondary Mortality 2 years No
Secondary Development of nephrotoxicity 2 years No
Secondary Use of galactomannan in this clinical context 2 years No
Secondary Time of administration of empirical antifungal therapy of broad-spectrum. 6 months No