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Accelerated Treatment of Endocarditis (POET II)

Primary Purpose

Endocarditis

Status
Recruiting
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Accelerated antibiotic treatment
Standard treatment length
Sponsored by
Herlev Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Endocarditis

Eligibility Criteria

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

Inclusion Criteria:

  • Admitted with infectious endocarditis (duke criteria) < 14 days of relevant antibiotic treatment for endocarditis One of the following bacteria: Streptococci, enterococcus faecalis, staphylococcus aureus

Exclusion Criteria:

  • Known immune incompetency, Relapse endocarditis with 6 months, Unable to give informed concent

Sites / Locations

  • RigshositaletRecruiting
  • Herlev HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Accelerated antibiotic treatment

Standard length of antibiotic treatment

Arm Description

Patients are treated shorter than usual

Patients are receiving the standard length of antibiotic treatment

Outcomes

Primary Outcome Measures

Combined endpoint of: All cause mortality, Bacteremia with primary pathogen, embolic episodes, not planned Heart surgery
The primary endpoint is a combined endpoint consisting of the following events occurring within six months after the earliest time of potential treatment discontinuation: Death; Embolisms; Bacteraemia with the same microorganism; Heart surgery not planned at the time of randomization.

Secondary Outcome Measures

Expenses associated with admission and treatment
Combined endpoint consisting of expenses due to i admission ii medication iii transportation iv surgery v imaging vi home care
Duration of admission
Duration of admission
Duration of antibiotic treatment
Duration of antibiotic treatment
Frequency of catheter complication
Frequency of catheter complication
Unplanned Heart surgery
• Unplanned cardiac valve surgery defined as any cardiac surgery which is not planned at the time of randomization. Data will be extracted from the electronic patient journal.
All cause mortality
All cause mortality
Embolic events
Embolic events
Re-bacteremia with the primary pathogen
• Relapse of bacteremia defined as a positive blood culture with the same microorganism as during the initial IE admission (streptococci spp., S. aureus, or E. faecalis). Data will be extracted from the electronic patient journal.

Full Information

First Posted
August 16, 2019
Last Updated
November 22, 2021
Sponsor
Herlev Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05144399
Brief Title
Accelerated Treatment of Endocarditis
Acronym
POET II
Official Title
Accelerated Treatment of Endocarditis
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2019 (Actual)
Primary Completion Date
October 31, 2022 (Anticipated)
Study Completion Date
October 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Herlev Hospital

4. Oversight

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

5. Study Description

Brief Summary
Existing guidelines recommend a duration of antibiotic treatment of endocarditis of 4-6 weeks one or more types of intravenously administered antibiotics. The long hospitalization increases several risks for the patient, including mental strain and increased loss of function. Furthermore, it poses a significant financial burden on the health systems. Current guidelines fail to use available clinical and paraclinical, data collected from patients (echo, temperature, CRP, leukocytes, procalcitonin etc.) to determine duration of treatment. A strategy including these data in treatment algorithms ensures an individualized treatment, targeting the individual patient's course and response to treatment. Thus, the purpose of this open-label, prospective, non-inferiority, RCT study is to investigate the safety and effectiveness of shortening treatment of endocarditis based on the individual patient's initial treatment response, sampling 750 patients, approx. 200 patients with each type of bacteria (Streptococci; Enterococcus faecalis; Staphylococcus aureus).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endocarditis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
750 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Accelerated antibiotic treatment
Arm Type
Experimental
Arm Description
Patients are treated shorter than usual
Arm Title
Standard length of antibiotic treatment
Arm Type
Other
Arm Description
Patients are receiving the standard length of antibiotic treatment
Intervention Type
Other
Intervention Name(s)
Accelerated antibiotic treatment
Intervention Description
E. faecalis uncomplicated: 4 weeks. E. faecalis complicated: 4 weeks. S. aureus uncomplicated: 2 weeks. S. aureus complicated: 4 weeks. Streptococci spp. NVE: 2 weeks. Streptococci spp. PVE or abscess: 3 weeks. Subsequent to cardiac surgery with a negative valve culture (organism NOT grown in laboratory from valve): Minimum 1 week after surgery regardless of previous antibiotic treatment received. Subsequent to cardiac surgery with a positive valve culture (organism grown in laboratory from valve): treatment will continue with the start date of antibiotics changed to the date of surgery. Complicated IE defined as patients with abscess, embolic event, surgically treated IE, and/or PVE. NVE: native valve endocarditis, PVE: prosthetic valve endocarditis.
Intervention Type
Other
Intervention Name(s)
Standard treatment length
Intervention Description
E. faecalis uncomplicated: 6 weeks. E. faecalis complicated: 6 weeks. S. aureus uncomplicated: 4 weeks. S. aureus complicated: 6 weeks. Streptococci spp. NVE: 4 weeks. Streptococci spp. PVE or abscess: 6 weeks. Subsequent to cardiac surgery with a negative valve culture (organism NOT grown in laboratory from valve): Minimum 2 weeks after surgery regardless of previous antibiotic treatment received. Subsequent to cardiac surgery with a positive valve culture (organism grown in laboratory from valve): treatment will continue with the start date of antibiotics changed to the date of surgery. Complicated IE defined as patients with abscess, embolic event, surgically treated IE, and/or PVE. NVE: native valve endocarditis, PVE: prosthetic valve endocarditis.
Primary Outcome Measure Information:
Title
Combined endpoint of: All cause mortality, Bacteremia with primary pathogen, embolic episodes, not planned Heart surgery
Description
The primary endpoint is a combined endpoint consisting of the following events occurring within six months after the earliest time of potential treatment discontinuation: Death; Embolisms; Bacteraemia with the same microorganism; Heart surgery not planned at the time of randomization.
Time Frame
6 months after randomization
Secondary Outcome Measure Information:
Title
Expenses associated with admission and treatment
Description
Combined endpoint consisting of expenses due to i admission ii medication iii transportation iv surgery v imaging vi home care
Time Frame
6 months after randomization
Title
Duration of admission
Description
Duration of admission
Time Frame
6 months after randomization
Title
Duration of antibiotic treatment
Description
Duration of antibiotic treatment
Time Frame
6 months after randomization
Title
Frequency of catheter complication
Description
Frequency of catheter complication
Time Frame
6 months after randomization
Title
Unplanned Heart surgery
Description
• Unplanned cardiac valve surgery defined as any cardiac surgery which is not planned at the time of randomization. Data will be extracted from the electronic patient journal.
Time Frame
6 months after randomization
Title
All cause mortality
Description
All cause mortality
Time Frame
6 months after randomization
Title
Embolic events
Description
Embolic events
Time Frame
6 months after randomization
Title
Re-bacteremia with the primary pathogen
Description
• Relapse of bacteremia defined as a positive blood culture with the same microorganism as during the initial IE admission (streptococci spp., S. aureus, or E. faecalis). Data will be extracted from the electronic patient journal.
Time Frame
6 months after randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Admitted with infectious endocarditis (duke criteria) < 14 days of relevant antibiotic treatment for endocarditis One of the following bacteria: Streptococci, enterococcus faecalis, staphylococcus aureus Exclusion Criteria: Known immune incompetency, Relapse endocarditis with 6 months, Unable to give informed concent
Facility Information:
Facility Name
Rigshositalet
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Henning Bundgaard
Phone
+4535450512
Email
henning.bundgaard@regionh.dk
Facility Name
Herlev Hospital
City
Herlev
ZIP/Postal Code
2730
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
kasper iversen
Phone
+4538686009
Email
kasper.karmark.iversen@regionh.dk

12. IPD Sharing Statement

Plan to Share IPD
No

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Accelerated Treatment of Endocarditis

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