- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00838643
Invasive Aspergillosis After Allogeneic Hematopoietic Stem Cell Transplantation (HSCT)
February 6, 2009 updated by: Ospedale Santa Croce-Carle Cuneo
Incidence of Invasive Aspergillosis in Allogeneic Stem Cell Transplantation Patients: an Italian Prospective Multicentre Study
Evaluation of incidence of invasive aspergillosis in patients who have undergone an allogeneic stem cell transplantation, with particular regard to the role of galactomannan assay and of early TC scan in asymptomatic patients.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Actual)
220
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Cuneo, Italy, 12100
- Azienda Sanitaria Ospedaliera santa Croce e Carle
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Adult patients given allogeneic HSCT in tertiary care centers or university hospitals in Piedmont
Description
Inclusion Criteria:
- Age > 16 years
- Allogeneic HSCT for a haematological disease
- Written informed consent to the study
Exclusion Criteria:
- Pediatric patients
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Allogeneic pts
Adult allogeneic HSCT recipients
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Incidence of invasive aspergillosis
Time Frame: 1 year
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Clinical applicability of the EORTC/MSG criteria in a prospective multicenter trial
Time Frame: 1 year
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2002
Primary Completion (Actual)
June 1, 2007
Study Completion (Anticipated)
December 1, 2009
Study Registration Dates
First Submitted
February 5, 2009
First Submitted That Met QC Criteria
February 5, 2009
First Posted (Estimate)
February 6, 2009
Study Record Updates
Last Update Posted (Estimate)
February 9, 2009
Last Update Submitted That Met QC Criteria
February 6, 2009
Last Verified
February 1, 2009
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Gal-01
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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