Prophylactic Piperacillin/Tazobactam in Hematopoietic Stem Cell Transplantation

Sponsor
Chinese PLA General Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT01714557
Collaborator
(none)
150
1
3
26
5.8

Study Details

Study Description

Brief Summary

Neutropenia is very common in patients received hematopoietic stem cell transplantation, with median duration of about 14 days. Almost all neutropenia will suffer from febrile without prophylactic antibiotics. IDSA recommended fluoroquinolones as prophylaxis in neutropenia patients of high risks, while in China, major pathogens possess high resistance to fluoroquinolones. It is not clear whether prophylaxis is of benefit, nor the appropriate prophylaxis regimen.

The current study will evaluate the three different regimen:
  1. No prophylaxic antibiotic

  2. Piperacillin as prophylaxis for neutropenia patients. Piperacillin has anti-pseudomonas activity.

  3. Piperacillin/tazobactam as prophylaxis for neutropenia patients. Piperacillin/tazobactam has highest susceptibility rate among common anti-pseudomonas antibiotics.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

  1. Swab culture (skin, pharyngeal, nasal, anus) when administered into laminar flow room after transplantation.

  2. Randomize the neutropenia patients into 3 groups.

  3. Receive 3 regimen.

  4. Full record of clinical data, including background diseases, previous antibiotics within 90 days, febrile or not at the TOC.

  5. For patients developed febrile, imipenem will be prescribed, even if the patient received no prophylaxis. At the same time, the follow-up ended.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Piperacillin/Tazobactam for Prophylaxis in Patients of Neutropenia After Hematopoietic Stem Cell Transplantation - A Pilot Study
Study Start Date :
Sep 1, 2012
Anticipated Primary Completion Date :
Sep 1, 2014
Anticipated Study Completion Date :
Nov 1, 2014

Arms and Interventions

Arm Intervention/Treatment
No Intervention: No prophylaxis

Active Comparator: piperacillin

Drug: Piperacillin
4.0g q8h 3-5 days

Experimental: piperacillin/tazobactam

Drug: Piperacillin-tazobactam combination product
4.5g q8h 3-5 days
Other Names:
  • Tazocin
  • Outcome Measures

    Primary Outcome Measures

    1. febrile rate [3 weeks after beginning of prophylaxis]

      In both group, how many patients developed febrile.

    Secondary Outcome Measures

    1. Microbiologic efficacy in febrile patients [3 weeks after beginning of prophylaxis]

      The success rate and failure rate will be calculated. The microbiologic culture is positive at 3 weeks of prophylaxis, showing pathogen sensitive to Piperacillin/tazobactam, the case will be evaluated as breakthrough infection, that means microbiologic failure. The microbiologic culture is negative at 3 weeks of prophylaxis,, or positive fungus or non-typical organisms, the case will be evaluated as microbiologic success.

    2. Recovery rate from neutropenia [3 weeks after beginning of prophylaxis]

      How many patients reached the ANC > 0.5×109/L more than 3 days.

    3. AE [3 weeks after beginning of prophylaxis]

      How many patients developed unexpected medical events.

    4. Cost of drug and hospital-stay [3 weeks after beginning of prophylaxis]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    13 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age 13-65 years

    • Received Autologous or Allogeneic hematopoietic stem cell transplantation.

    • ECOG score 0-1.

    • ICF is available.

    Exclusion Criteria:
    • Allergic to any therapy drug.

    • Documented infection before neutropenia.

    • Renal dysfunction.

    • Suffering from central nervous system or mental disease.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Chinese PLA general hospital Beijing Beijing China

    Sponsors and Collaborators

    • Chinese PLA General Hospital

    Investigators

    • Principal Investigator: wenrong huang, Doctor, Employee

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Wenrong Huang, Associate director, Hematology, Chinese PLA General hospital, Chinese PLA General Hospital
    ClinicalTrials.gov Identifier:
    NCT01714557
    Other Study ID Numbers:
    • TZP-HEM-20120608
    First Posted:
    Oct 26, 2012
    Last Update Posted:
    Oct 26, 2012
    Last Verified:
    Oct 1, 2012

    Study Results

    No Results Posted as of Oct 26, 2012