Trial of Levofloxacin as Prophylaxis After Allogeneic Stem Cell Transplantation (SCT)

NCT ID: NCT00215007

Last Updated: 2007-11-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE2/PHASE3

Study Classification

INTERVENTIONAL

Brief Summary

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The purpose of this study is to evaluate the efficacy of levofloxacin to prevent bacterial infections in the postneutropenic period in patients who have undergone allogeneic stem cell transplantation (SCT).

Detailed Description

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Conditions

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Malignancy Allogeneic Stem Cell Transplantation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Interventions

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Levofloxacin

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Allogeneic SCT
* Postneutropenic period
* Written consent

Exclusion Criteria

* Fever
* Antibiotic therapy
* Neutropenia
* Refusal by the patient
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Charite University, Berlin, Germany

OTHER

Sponsor Role lead

Principal Investigators

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Igor Wolfgang Blau, Dr.

Role: STUDY_CHAIR

Charite, CBF, Berlin, Germany

Locations

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Charite, CBF

Berlin, State of Berlin, Germany

Site Status RECRUITING

Countries

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Germany

Central Contacts

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Igor Wolfgang Blau, Dr.

Role: CONTACT

Phone: 0049 30 8445 4430

Email: [email protected]

Martin Schmidt-Hieber, Dr.

Role: CONTACT

Phone: 0049 30 8445 4555

Email: [email protected]

Facility Contacts

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Igor Wolfgang Blau

Role: primary

Other Identifiers

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Levosta-CBF-02/04

Identifier Type: -

Identifier Source: org_study_id