Intravenous Pentamidine for Pneumocystis Jirovecii Pneumonia

Sponsor
University of Illinois at Chicago (Other)
Overall Status
Completed
CT.gov ID
NCT02669706
Collaborator
(none)
50
1
15
3.3

Study Details

Study Description

Brief Summary

The main objective of this study is to assess the safety of administering intravenous (IV) pentamidine for Pneumocystis jirovecii pneumonia (PJP) prophylaxis in adult inpatients with hematologic malignancies and stem cell transplant recipients. There will also be an assessment of patient satisfaction associated with intravenous pentamidine PJP prophylactic therapy.

Condition or Disease Intervention/Treatment Phase

Detailed Description

This study is a prospective, single arm study to assess safety of IV pentamidine for PJP prophylaxis. Patient satisfaction associated with IV pentamidine will also be assessed using a survey adapted from the validated Treatment Satisfaction Questionnaire for Medication (version 1.4).

Adult patients with a hematologic malignancy or who are receiving or have received a stem-cell transplant at the University of Illinois Hospitals and Clinics who have an indication for PJP prophylaxis therapy. They will receive intravenous pentamidine during their planned admissions for chemotherapy when they have an indication for and/or are due to receive pentamidine prophylaxis. These patients are outlined below in the inclusion criteria. Patients may or may not have received aerosolized or IV pentamidine prior to inclusion in the study.

Eligible patients will receive IV pentamidine during hospital admissions. Patients will be routinely monitored by nursing staff during and after the infusion. Nursing staff will monitor the systolic and diastolic blood pressure at baseline and one hour post infusion. Patients will also be monitored for nausea/vomiting. Patients who receive IV pentamidine will have anti-emetics available on call to use in the event that they become nauseous. Data will be collected on the type, grade, and incidence of adverse effects by research personnel.

Study Design

Study Type:
Observational
Actual Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Assessment of the Safety and Intravenous Pentamidine for Pneumocystis Jirovecii Pneumonia in Patients With Hematologic Malignancies and Stem Cell Transplant Recipients.
Study Start Date :
Mar 1, 2015
Actual Primary Completion Date :
May 1, 2016
Actual Study Completion Date :
Jun 1, 2016

Arms and Interventions

Arm Intervention/Treatment
IV pentamidine

Pentamidine 4mg/kg IV every month (maximum 300mg)

Drug: Pentamidine
Pentamidine is an antimicrobial medication given for prevention and treatment of Pneumocystis pneumonia (PJP) caused by Pneumocystis jirovecii
Other Names:
  • NebuPent
  • Pentam
  • Outcome Measures

    Primary Outcome Measures

    1. Safety of IV pentamidine for PJP prophylaxis [1 year]

      Safety will be assessed via analyzing the number of patients experiencing adverse effects, with their severity graded using CTCAE v4.0.

    Secondary Outcome Measures

    1. Number of confirmed cases of PJP diagnosed [1 year]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Adults (18 years or older)

    • Hematologic malignancy diagnosis or stem-cell transplant recipient

    • Eligible for PJP prophylaxis therapy at time of enrollment as per institutional guidelines in compliance with NCCN guidelines. These patients include:

    • Acute myeloid leukemia patients receiving induction and consolidation (first line and relapsed/refractory)

    • Acute lymphoid leukemia patients receiving HyperCVAD/R (cyclophosphamide, vincristine, doxorubicin, dexamethasone, methotrexate, cytarabine, rituximab)

    • Lymphoma patients receiving ICE (ifosfamide, carboplatin, etoposide), DA-R-EPOCH (dose-adjusted rituximab, etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin), and other inpatient lymphoma regimens

    • Patients receiving other inpatient chemotherapy regimens that are given on a monthly basis

    • Patients who have received an allogeneic stem cell transplant

    • Have given informed consent

    • May have previously received inhaled or IV pentamidine

    Exclusion Criteria:
    • Pregnancy

    • Prisoners

    • Patients with a documented allergy or hypersensitivity to pentamidine.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Illinois Hospital and Health Sciences System Chicago Illinois United States 60612

    Sponsors and Collaborators

    • University of Illinois at Chicago

    Investigators

    • Principal Investigator: Jennifer Anderson, PharmD, University of Illinois at Chicago

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Jennifer Anderson, PharmD, University of Illinois at Chicago
    ClinicalTrials.gov Identifier:
    NCT02669706
    Other Study ID Numbers:
    • 2014-1000
    First Posted:
    Feb 1, 2016
    Last Update Posted:
    Jun 30, 2016
    Last Verified:
    Jun 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 30, 2016