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Hyperbaric Oxygen Treatment in Humans With Gram Positive Cocci Endocarditis (ENDOHOT)

Primary Purpose

Infectious Endocarditis

Status
Unknown status
Phase
Phase 2
Locations
Denmark
Study Type
Interventional
Intervention
Hyperbaric oxygen
Sponsored by
Ole Hyldegaard
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infectious Endocarditis

Eligibility Criteria

18 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Left sided IE with gram positive cocci.
  2. IE has been diagnosed according to modified Duke Criteria.
  3. Patients must be stable, by means of no need for hemodynamic pressure support.
  4. The patient must be able to be seated for the 1.5 hour the HBOT at least two times a day for 3 days.
  5. The patient must be able to perform Valsalva's - or Frenzels manoeuvre - to equalize middle ear pressure. As prophylaxis, all patients will receive detumescent nose drops as Otrivin® to facilitate ear- and sinuses equilibration. In the rare event it is still not possible for the patient to equalize pressure, a paracentesis or drainage of the tympanic membrane must be performed by the ear-nose and throat (ENT) doctor. All according to daily practice.
  6. The upstart of HBOT must be within the first 2 weeks of relevant antibiotic IE therapy.
  7. If a central venous catheter has been inserted, a chest X-ray must confirm no suspicion of pneumothorax.
  8. Patients must be >18-years old.

Exclusion Criteria:

  1. Claustrophobia that cannot be reversed by mild sedatives.
  2. Patients requiring mechanical ventilation.
  3. Undrained pneumothorax
  4. Pregnancy
  5. Unable to follow and understand simple commands
  6. Non-compliant

Sites / Locations

  • RigshospitaletRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

HBOT

Arm Description

Hyperbaric oxygen breathing at 2.4 atm.abs for 90 minutes. The course of hyperbaric oxygen treatment comprises a total of 6 pressure exposures, distributed 2 times daily, for 3 days.

Outcomes

Primary Outcome Measures

Changes in baseline characteristics with definite IE.
Standard clinical assesments of IE and paraclinical data

Secondary Outcome Measures

Full Information

First Posted
December 18, 2020
Last Updated
December 30, 2020
Sponsor
Ole Hyldegaard
Collaborators
Rigshospitalet, Denmark, Herlev Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04691440
Brief Title
Hyperbaric Oxygen Treatment in Humans With Gram Positive Cocci Endocarditis
Acronym
ENDOHOT
Official Title
Hyperbaric Oxygen Treatment in Humans With Gram Positive Cocci Endocarditis"
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Unknown status
Study Start Date
December 1, 2019 (Actual)
Primary Completion Date
July 1, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Ole Hyldegaard
Collaborators
Rigshospitalet, Denmark, 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
Infectious endocarditis (IE) is defined as an infection anywhere on the endocardium, most often localised to the cardiac valves. It is an infection with an increasing incidence and in Denmark with 6-700 new cases annually. Approximately 45% of the patients must undergo cardiac surgery with replacement of infected cardiac valves by prosthetic valves. Recently, the formation of biofilms infections has drawn attention with respect to the effects of hyperbaric re-oxygenation of stricken tissues as anaerobic bacterial metabolism with low levels of activity within the biofilm environment, may be responsible for the development of antimicrobial resistance. Polymorphonuclear leukocytes (PMNs) consume available oxygen in the conversion of oxygen to ROS and in the formation of reactive nitrogen species (RNS) by inducible nitric oxide (iNOS) as PMN's are activated by bacteria. In pre-clinical context the effect of hyperbaric oxygen treatment (HBOT) in re-oxygenating biofilm related infections have been demonstrated in infected lungs with Pseudomonas aeruginosa and staphylococcus aureus endocarditis. Adjunctive HBOT has never been offered to patients with IE. However, HBOT may be associated with reduced compliance and side effects, such as equalisation problems of ears and sinuses and confinement anxiety, and the treatment is organizational challenging. On this basis the investigators suggest an initial feasibility study as the basis for a later and larger scaled randomized controlled trial of HBOT in patients with IE.
Detailed Description
During antibiotic treatments with the indicated antibiotics the susceptible bacteria are subjected to metabolic changes of the Krebs cycles leading to intrabacterial accumulation of toxic hydroxyl oxygen radicals. The intrabacterial toxic reactive oxygen species (ROS) can subsequently react with DNA, lipids or proteins resulting in damages of those bacterial components adding to the killing of the bacteria. A consequence is that bactericidal antibiotics have reduced activity in infectious foci with poor oxygen supply like in abscesses or in biofilm infections as in IE and/or rapid consumption of oxygen due to PMN influx. The bacterial damages may, if killing is not obtained, result in mutations and selection of antibiotic resistant mutants. However, these discoveries also provide a possibility for improving the antibacterial effect by increasing the oxygen pressure in the infectious focus. This can be obtained by increasing oxygen tension in the tissues by treating the patients with HBOT - and have been shown in vitro and in vivo pre-clinical experiments. Exposing Pseudomonas aeruginosa biofilm models in vitro to HBOT has proved effective by significantly increasing the bactericidal effect of ciprofloxacin. More important, in an animal (rats) model of left-sided S. aureus IE on the aortic valves, tobramycin killing effect was significantly improved by adding HBOT as adjunctive therapy. Moreover, the rats revealed a reduced inflammatory response and improved clinical scores. No side effects were recorded during that study. In addition, the HBOT is also believed to improve the antibacterial effect of the PMNs, and thereby add to an enhanced elimination of infectious focus. This is being estimated by measurements of the respiratory burst of the PMNs, as well as their phagocytic capacity right before and right after the HBOT.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
HBOT
Arm Type
Experimental
Arm Description
Hyperbaric oxygen breathing at 2.4 atm.abs for 90 minutes. The course of hyperbaric oxygen treatment comprises a total of 6 pressure exposures, distributed 2 times daily, for 3 days.
Intervention Type
Drug
Intervention Name(s)
Hyperbaric oxygen
Intervention Description
The course of hyperbaric oxygen treatment comprises a total of 6 pressure exposures, distributed 2 times daily, for 3 days.
Primary Outcome Measure Information:
Title
Changes in baseline characteristics with definite IE.
Description
Standard clinical assesments of IE and paraclinical data
Time Frame
Up to 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Left sided IE with gram positive cocci. IE has been diagnosed according to modified Duke Criteria. Patients must be stable, by means of no need for hemodynamic pressure support. The patient must be able to be seated for the 1.5 hour the HBOT at least two times a day for 3 days. The patient must be able to perform Valsalva's - or Frenzels manoeuvre - to equalize middle ear pressure. As prophylaxis, all patients will receive detumescent nose drops as Otrivin® to facilitate ear- and sinuses equilibration. In the rare event it is still not possible for the patient to equalize pressure, a paracentesis or drainage of the tympanic membrane must be performed by the ear-nose and throat (ENT) doctor. All according to daily practice. The upstart of HBOT must be within the first 2 weeks of relevant antibiotic IE therapy. If a central venous catheter has been inserted, a chest X-ray must confirm no suspicion of pneumothorax. Patients must be >18-years old. Exclusion Criteria: Claustrophobia that cannot be reversed by mild sedatives. Patients requiring mechanical ventilation. Undrained pneumothorax Pregnancy Unable to follow and understand simple commands Non-compliant
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ole Hyldegaard, MD, PHD
Phone
+4535454092
Email
ole.hyldegaard@regionh.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Mia Pries-Heje, MD
Email
Mia Marie Pries-Heje <mia.marie.pries-heje.01@regionh.dk>
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ole Hyldegaard, MD, PHD
Organizational Affiliation
Rigshospitalet, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rigshospitalet
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mia Pries-Heje, MD

12. IPD Sharing Statement

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Hyperbaric Oxygen Treatment in Humans With Gram Positive Cocci Endocarditis

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