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Optimal Dosing of Vancomycin in an Adult Population of Hemato-oncology (Hemato-Vanco)

Primary Purpose

Vancomycin, Hematologic Malignancies, Febrile Neutropenia

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Additional blood sample
Sponsored by
Ciusss de L'Est de l'Île de Montréal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Vancomycin focused on measuring Bayesian model, Pharmacokinetics

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Subjects aged 18 and over;
  • Subjects diagnosed with a hematologic cancer;
  • Subjects hospitalized at Maisonneuve-Rosemont hospital between February 2021 and August 2021;
  • Intravenous vancomycin treatment prescribed by a doctor;
  • Subjects received at least 3 doses of intravenous vancomycin.

Exclusion Criteria:

  • Non-malignant diagnosis (aplastic anemia and rare metabolic diseases);
  • Subjects admitted to a critical care unit;
  • End-stage renal disease (GFR < 15 mL/min/1.73m2);
  • Patients undergoing dialysis/renal replacement therapy;
  • Acute kidney injury at the moment of the first vancomycin dosage (definition adapted from KDIGO criteria):

    1. Increase in serum creatinine by ≥ 26.5 umol/L within 48 hours or
    2. Increase in serum creatinine to ≥ 1.5 times baseline within prior 7 days
  • Pregnant women;
  • Severely burn patients;
  • Inability to give free and informed consent.

Sites / Locations

  • Maisonneuve-Rosemont HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Vancomycin

Arm Description

Subjects with hematologic cancer who received intravenous vancomycin for a suspected or confirmed infection.

Outcomes

Primary Outcome Measures

Pharmacokinetic Parameters : Volume of Distribution
Estimated from vancomycin serum concentrations and patient characteristics
Pharmacokinetic Parameters : Vancomycin clearance
Estimated from vancomycin serum concentrations and patient characteristics

Secondary Outcome Measures

Area Under the concentration-time Curve (AUC)
Serum Vancomycin Through Concentration
Vancomycin concentration measured just before the next infusion
Serum Vancomycin Peak Concentration
Vancomycin concentration measured 1 hour after the end of vancomycin infusion
Serum Vancomycin Elimination Phase Concentration
Vancomycin concentration measured 3 to 5 hours after the end of vancomycin infusion

Full Information

First Posted
February 9, 2021
Last Updated
February 12, 2021
Sponsor
Ciusss de L'Est de l'Île de Montréal
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1. Study Identification

Unique Protocol Identification Number
NCT04758442
Brief Title
Optimal Dosing of Vancomycin in an Adult Population of Hemato-oncology
Acronym
Hemato-Vanco
Official Title
Optimal Dosing of Vancomycin in an Adult Population of Hemato-oncology: a Nomogram Based on a Bayesian Population Model to Predict Initial Dosage of Vancomycin
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2021 (Actual)
Primary Completion Date
October 31, 2021 (Anticipated)
Study Completion Date
October 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ciusss de L'Est de l'Île de Montréal

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a single-center prospective pharmacokinetic study. The principal objective is to collect new data among patients with hematologic cancer to develop a Bayesian population pharmacokinetic model and to improve dose adjustment of intravenous vancomycin. Approximately 40 subjects meeting the inclusion and no exclusion criteria will be enrolled in the study. Vancomycin blood concentration will be measured at steady-state at three different moment for each participant : immediately before the infusion, 1 hour after the infusion and during the elimination phase (at 3, 4 or 5 hours after the infusion). This additional vancomycin serum concentration in the elimination phase will be used to estimate more precisely the vancomycin pharmacokinetic parameters in this specific population including the distribution volume and the elimination of the molecule. Ultimately, the purpose of this study is to create a nomogram to predict the optimal initial vancomycin dosing in adult patients with a hematologic cancer.
Detailed Description
STUDY DESIGN: Prospective, monocentric, pharmacokinetic study. Adults who have been diagnosed with a hematologic malignancy, are hospitalized at Maisonneuve-Rosemont hospital and received at least 3 doses of intravenous vancomycin. Pharmacokinetic parameters: Serum vancomycin concentration measured at steady state just before the beginning of the infusion (trough), 1 hour after completion of the infusion (peak) and between 3 to 5 hours after the end of the infusion (additional blood draw during the elimination phase). RECRUITMENT PROCESS: A systematic daily screening of hospitalized patients diagnosed with a hematologic cancer will be made by the research team and the pharmacists 7 days a week. An information sheet will be given to all potential eligible patients at their admission. When intravenous vancomycin is prescribed, a member of the research team will explain the study and present the Information and Consent Form (ICF) to the potential participant to obtain his/her official informed consent. DATA COLLECTION: Three blood draws will be planned around the fourth or fifth dose of vancomycin and collected by the nursing team. The sampling scheme is as follows: just before the beginning of the infusion (trough), 1 hour after completion of the infusion (peak) and 3, 4 or 5 hours after the end of the infusion (additional blood draw during the elimination phase) according to the assigned time of the participant. The assigned time of the additional blood draw will be randomized at the inclusion of the subject in the study. A member of the research team will provide the tubes to the nurse, will write and save sampling times and will ship the blood samples to the laboratory.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vancomycin, Hematologic Malignancies, Febrile Neutropenia
Keywords
Bayesian model, Pharmacokinetics

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Vancomycin
Arm Type
Experimental
Arm Description
Subjects with hematologic cancer who received intravenous vancomycin for a suspected or confirmed infection.
Intervention Type
Other
Intervention Name(s)
Additional blood sample
Intervention Description
Included subjects will provided three blood samples to follow vancomycin concentration
Primary Outcome Measure Information:
Title
Pharmacokinetic Parameters : Volume of Distribution
Description
Estimated from vancomycin serum concentrations and patient characteristics
Time Frame
During intravenous vancomycin treatment assessed to 72 hours
Title
Pharmacokinetic Parameters : Vancomycin clearance
Description
Estimated from vancomycin serum concentrations and patient characteristics
Time Frame
During intravenous vancomycin treatment assessed to 72 hours
Secondary Outcome Measure Information:
Title
Area Under the concentration-time Curve (AUC)
Time Frame
between 0 to 24 hours during vancomycin administration
Title
Serum Vancomycin Through Concentration
Description
Vancomycin concentration measured just before the next infusion
Time Frame
5 minutes before the selected infusion
Title
Serum Vancomycin Peak Concentration
Description
Vancomycin concentration measured 1 hour after the end of vancomycin infusion
Time Frame
60 minutes after the end of the infusion
Title
Serum Vancomycin Elimination Phase Concentration
Description
Vancomycin concentration measured 3 to 5 hours after the end of vancomycin infusion
Time Frame
3 to 5 hours after the end of the infusion (+/- 30 minutes)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects aged 18 and over; Subjects diagnosed with a hematologic cancer; Subjects hospitalized at Maisonneuve-Rosemont hospital between February 2021 and August 2021; Intravenous vancomycin treatment prescribed by a doctor; Subjects received at least 3 doses of intravenous vancomycin. Exclusion Criteria: Non-malignant diagnosis (aplastic anemia and rare metabolic diseases); Subjects admitted to a critical care unit; End-stage renal disease (GFR < 15 mL/min/1.73m2); Patients undergoing dialysis/renal replacement therapy; Acute kidney injury at the moment of the first vancomycin dosage (definition adapted from KDIGO criteria): Increase in serum creatinine by ≥ 26.5 umol/L within 48 hours or Increase in serum creatinine to ≥ 1.5 times baseline within prior 7 days Pregnant women; Severely burn patients; Inability to give free and informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Annie Brisebois-Boyer, Pharm.D, M. Sc
Phone
514-252-3400
Ext
1553
Email
abriseboisboyer.hmr@ssss.gouv.qc.ca
First Name & Middle Initial & Last Name or Official Title & Degree
TEAM HEMATO-VANCO, Pharm. D
Phone
514-252-3400
Ext
6124
Email
residents.phm2021.cemtl@ssss.gouv.qc.ca
Facility Information:
Facility Name
Maisonneuve-Rosemont Hospital
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H1T 2M4
Country
Canada
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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Optimal Dosing of Vancomycin in an Adult Population of Hemato-oncology

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