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Partial Oral Treatment of Endocarditis (POET)

Primary Purpose

Endocarditis

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Oral treatment with antibiotics for endocarditis
Guideline treatment with parenteral antibiotics
Sponsored by
Rigshospitalet, Denmark
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:

  • Left-sided endocarditis based on the Duke criteria
  • Infected with one of the following microorganisms:

    • Streptococci
    • Enterococcus faecalis
    • Staphylococcus aureus
    • Coagulase-negative staphylococci.
  • ≥ 18 years
  • At least 10 days of appropriate parenteral antibiotic treatment overall, and at least 1 week of appropriate parenteral treatment after valve surgery
  • Afebrile (T < 38.0) > 2 days
  • Decreasing infection parameters (CRP dropped to less than 25% of peak value or < 20 mg/l, and white blood cell count < 15 x 109/l) during antibiotic treatment
  • No sign of abscess formation by echocardiography
  • Transthoracic and transoesophageal echocardiography performed within 48 hours prior to randomization

Exclusion Criteria:

  • Body mass index > 40
  • Concomitant infection requiring intravenous antibiotic therapy
  • Inability to give informed consent to participation
  • Suspicion of reduced absorption of oral treatment due to abdominal disorder
  • Reduced compliance

Sites / Locations

  • Aalborg Sygehus
  • Skejby Sygehus
  • Rigshospitalet
  • Gentofte Hospital
  • Herlev Hoslpital
  • Hillerød Hospital
  • Odense Sygehus
  • Roskilde Sygehus

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Guideline treatment with parenteral antibiotics

Oral treatment with antibiotics

Arm Description

Guideline treatment with parenteral antibiotics

Oral treatment with antibiotics based on resistens pattern

Outcomes

Primary Outcome Measures

The primary endpoint is a composite endpoint including all cause mortality, unplanned cardiac surgery, embolic events and relapse of positive blood cultures with the primary pathogen

Secondary Outcome Measures

Quality of life
QOL performed during the study and after completion of the study
Cost of treatment
Duration of antibiotic therapy
Complications related to intravenous catheter

Full Information

First Posted
June 13, 2011
Last Updated
March 9, 2019
Sponsor
Rigshospitalet, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT01375257
Brief Title
Partial Oral Treatment of Endocarditis
Acronym
POET
Official Title
Partial Oral Treatment of Endocarditis
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
July 2011 (Actual)
Primary Completion Date
August 30, 2017 (Actual)
Study Completion Date
August 30, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background Current management of infective endocarditis include admission and treatment with parenteral antibiotics for 4 weeks - 6 weeks. Resource demands and psychological issues of present management strategy make it highly relevant to seek for alternative more lenient alternatives. Experiences with oral treatment are only sporadically described, but observational data suggest that oral treatment could be a feasible option. The investigators have in 2010 treated 12 endocarditis patients with partial oral antibiotics with a 100% success rate. Study design The POET study is a Danish multicenter, prospective, randomized, open label study. The primary aim is to show non-inferiority of partial oral treatment with antibiotics of endocarditis compared to full parenteral treatment. Stable patients (n=400) with streptococci, staphylococci or enterococci infecting the mitral valve or the aortic valve will be included. After a minimum of 10 days of parenteral treatment, patients will be randomized to oral therapy or parenteral therapy. Special recommendations for oral treatment have been developed based on expected minimal inhibitory concentrations and pharmacokinetic calculations. Patients will be followed for 6 months after completion of antibiotic therapy. The primary endpoint is a composition of all cause mortality, unplanned cardiac surgery, embolic events and relapse of positive blood cultures with the primary pathogen.

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
400 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Guideline treatment with parenteral antibiotics
Arm Type
Active Comparator
Arm Description
Guideline treatment with parenteral antibiotics
Arm Title
Oral treatment with antibiotics
Arm Type
Experimental
Arm Description
Oral treatment with antibiotics based on resistens pattern
Intervention Type
Drug
Intervention Name(s)
Oral treatment with antibiotics for endocarditis
Intervention Type
Drug
Intervention Name(s)
Guideline treatment with parenteral antibiotics
Primary Outcome Measure Information:
Title
The primary endpoint is a composite endpoint including all cause mortality, unplanned cardiac surgery, embolic events and relapse of positive blood cultures with the primary pathogen
Time Frame
Approximately 7 months. From randomisation until 6 months after end of study medication
Secondary Outcome Measure Information:
Title
Quality of life
Description
QOL performed during the study and after completion of the study
Time Frame
Approximately 7 months. From randomisation until 6 months after end of study medication
Title
Cost of treatment
Time Frame
Approximately 7 months. From randomisation until 6 months after end of study medication
Title
Duration of antibiotic therapy
Time Frame
Approximately 7 months. From randomisation until 6 months after end of study medication
Title
Complications related to intravenous catheter
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Left-sided endocarditis based on the Duke criteria Infected with one of the following microorganisms: Streptococci Enterococcus faecalis Staphylococcus aureus Coagulase-negative staphylococci. ≥ 18 years At least 10 days of appropriate parenteral antibiotic treatment overall, and at least 1 week of appropriate parenteral treatment after valve surgery Afebrile (T < 38.0) > 2 days Decreasing infection parameters (CRP dropped to less than 25% of peak value or < 20 mg/l, and white blood cell count < 15 x 109/l) during antibiotic treatment No sign of abscess formation by echocardiography Transthoracic and transoesophageal echocardiography performed within 48 hours prior to randomization Exclusion Criteria: Body mass index > 40 Concomitant infection requiring intravenous antibiotic therapy Inability to give informed consent to participation Suspicion of reduced absorption of oral treatment due to abdominal disorder Reduced compliance
Facility Information:
Facility Name
Aalborg Sygehus
City
Aalborg
Country
Denmark
Facility Name
Skejby Sygehus
City
Aarhus
ZIP/Postal Code
8200
Country
Denmark
Facility Name
Rigshospitalet
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Facility Name
Gentofte Hospital
City
Copenhagen
Country
Denmark
Facility Name
Herlev Hoslpital
City
Copenhagen
Country
Denmark
Facility Name
Hillerød Hospital
City
Hillerød
Country
Denmark
Facility Name
Odense Sygehus
City
Odense
ZIP/Postal Code
5000
Country
Denmark
Facility Name
Roskilde Sygehus
City
Roskilde
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
35349038
Citation
Bundgaard JS, Iversen K, Pries-Heje M, Ihlemann N, Gill SU, Madsen T, Elming H, Povlsen JA, Bruun NE, Hofsten DE, Fuursted K, Christensen JJ, Schultz M, Rosenvinge F, Helweg-Larsen J, Kober L, Torp-Pedersen C, Fosbol EL, Tonder N, Moser C, Bundgaard H, Mogensen UM. Self-assessed health status and associated mortality in endocarditis: secondary findings from the POET trial. Qual Life Res. 2022 Sep;31(9):2655-2662. doi: 10.1007/s11136-022-03126-x. Epub 2022 Mar 29.
Results Reference
derived
PubMed Identifier
30152252
Citation
Iversen K, Ihlemann N, Gill SU, Madsen T, Elming H, Jensen KT, Bruun NE, Hofsten DE, Fursted K, Christensen JJ, Schultz M, Klein CF, Fosboll EL, Rosenvinge F, Schonheyder HC, Kober L, Torp-Pedersen C, Helweg-Larsen J, Tonder N, Moser C, Bundgaard H. Partial Oral versus Intravenous Antibiotic Treatment of Endocarditis. N Engl J Med. 2019 Jan 31;380(5):415-424. doi: 10.1056/NEJMoa1808312. Epub 2018 Aug 28.
Results Reference
derived
PubMed Identifier
23351813
Citation
Iversen K, Host N, Bruun NE, Elming H, Pump B, Christensen JJ, Gill S, Rosenvinge F, Wiggers H, Fuursted K, Holst-Hansen C, Korup E, Schonheyder HC, Hassager C, Hofsten D, Larsen JH, Moser C, Ihlemann N, Bundgaard H. Partial oral treatment of endocarditis. Am Heart J. 2013 Feb;165(2):116-22. doi: 10.1016/j.ahj.2012.11.006. Epub 2013 Jan 3.
Results Reference
derived

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Partial Oral Treatment of Endocarditis

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