UARK 2009-99 A Non-interventional Observational Study of Infectious Complications in Cancer Patients

Sponsor
University of Arkansas (Other)
Overall Status
Withdrawn
CT.gov ID
NCT01622595
Collaborator
(none)
0
1
73
0

Study Details

Study Description

Brief Summary

OBSERVATIONAL STUDY OF INFECTIOUS COMPLICATIONS IN CANCER PATIENTS

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    A NON-INTERVENTIONAL, OBSERVATIONAL STUDY OF INFECTIOUS COMPLICATIONS IN CANCER PATIENTS

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    0 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Retrospective
    Official Title:
    A Non-interventional Observational Study of Infectious Complications in Cancer Patients
    Study Start Date :
    Nov 1, 2009
    Anticipated Primary Completion Date :
    Dec 1, 2015
    Anticipated Study Completion Date :
    Dec 1, 2015

    Outcome Measures

    Primary Outcome Measures

    1. To study the incidence, risk factors, clinical presentation, diagnosis and prognostic factors of infectious complications in cancer patients [3 years]

      To study the incidence, risk factors, clinical presentation, diagnosis and prognostic factors of infectious complications in cancer patients

    Secondary Outcome Measures

    1. incidence [3 years]

      To determine the overall incidence of different infections, including bacterial, fungal and viral infections in cancer patients receiving chemotherapy and / or hematopoietic stem cell transplantation. To describe the natural history of such infections in cancer patients. To monitor the adherence of Myeloma institute for research and therapy(MIRT) health care workers to the MIRT standard operational procedures (SOPs) To identify risk factors for the development of specific infections. To validate surrogate markers as early diagnostic tools for various infections.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • cancer patients with Infections
    Exclusion Criteria:
    • No Infections

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Arkansas for Medical Sciences Little Rock Arkansas United States 72205

    Sponsors and Collaborators

    • University of Arkansas

    Investigators

    • Principal Investigator: Senu Apewokin, MD, UAMS

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Arkansas
    ClinicalTrials.gov Identifier:
    NCT01622595
    Other Study ID Numbers:
    • 112265
    First Posted:
    Jun 19, 2012
    Last Update Posted:
    Oct 27, 2015
    Last Verified:
    Oct 1, 2015
    Keywords provided by University of Arkansas
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 27, 2015