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The Oral Microbiota as Reservoir for Systemic Opportunistic Pathogens

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ClinicalTrials.gov Identifier: NCT02619903
Recruitment Status : Completed
First Posted : December 2, 2015
Last Update Posted : June 25, 2021
Sponsor:
Collaborator:
Lund University
Information provided by (Responsible Party):
Daniel Joensson, Malmö University

Brief Summary:

Small pilot studies with approximately 20 people per group support that eradication of the oral flora causes fewer exacerbations in chronic obstructive pulmonary disease (COPD) patients. The biological underpinning put forward is that eradicating the oral microbiome will eliminate a source of re-infection as the concentration of antibiotics prescribed to treat COPD exacerbations are not able to inhibit the bacteria in the oral biofilms that require 250 times higher concentration.

The specific aim is to investigate if adding advanced dental cleaning to COPD treatment can (i) lower the number of exacerbations and (ii) improve the COPD symptoms the coming 12 months. In an effort to explain the underpinning mechanism we will collect oral dental biofilm samples at baseline and follow up in the treatment and control group to investigate changes in the composition of the biofilm.

The subjects are selected by experienced COPD nurses. Exclusion criteria are having metastatic cancer or dementia. The COPD clinic informs the dental personal about COPD parameters, including spirometry data. At the dental clinic the patient answers a questionnaire, including a COPD assessment test (CAT) which has been validated extensively. The patients undergo a dental examination and are then randomized to test or control group. The test group go through supra- and subgingival scaling and scraping of the tongue as well as chlorhexidine rinse. The control group attends all visits.

All subjects go through the intervention after 6 months and are followed up after 12 and 24 months using questionnaire, dental plaque sampling and spirometry. The COPD nurses reviewing their medical records assess number of exacerbations.

A confirmation of the study hypothesis will be important in lowering the number of exacerbations in COPD patients, causing less suffering, less costs and less usage of antibiotics. If dental treatment is beneficial for exacerbation frequency it could be argued that dental treatment should be subsidized in this patient category.


Condition or disease Intervention/treatment Phase
COPD Exacerbation Pulmonary Disease, Chronic Obstructive Dental Plaque Procedure: Dental cleaning Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 101 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Test versus control for dental treatment in attenuating exacerbations in COPD.
Masking: Double (Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: The Oral Microbiota as Reservoir for Systemic Opportunistic Pathogens
Study Start Date : February 2016
Actual Primary Completion Date : December 31, 2020
Actual Study Completion Date : December 31, 2020

Arm Intervention/treatment
No Intervention: COPD Control
Subjects with COPD recieve no treatment. When exiting the trial after 12 months, they do however receive the intervention.
Active Comparator: COPD Test
Subjects with COPD that do get the additional dental cleaning, as well as dental examination.
Procedure: Dental cleaning
Dental scaling and cleaning to remove dental plaque as well as removing the tongue biofilm.




Primary Outcome Measures :
  1. COPD exacerbations in 12 months [ Time Frame: 12 months ]
    We will ask the patients how many exacerbations they had and go through medical records.


Secondary Outcome Measures :
  1. COPD symptoms [ Time Frame: 12 months ]
    COPD symptoms based on CAT-score (COPD Assessment Test)


Other Outcome Measures:
  1. Changes in oral microbiome [ Time Frame: 12 months ]
    Changes in the oral plaque microbiota comparing baseline and 12 months.



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • COPD arm - COPD Gold standard 1-4.

Exclusion Criteria:

  • Physically unable to make it to the dental clinic.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02619903


Locations
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Sweden
Folktandvarden Skane
Malmo, Sweden
Orebro Specialisttandvard
Orebro, Sweden
Sponsors and Collaborators
Malmö University
Lund University
Investigators
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Principal Investigator: Daniel Jönsson, DDS, PhD Lund University
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Responsible Party: Daniel Joensson, Assistant professor, Malmö University
ClinicalTrials.gov Identifier: NCT02619903    
Other Study ID Numbers: 2015-279
First Posted: December 2, 2015    Key Record Dates
Last Update Posted: June 25, 2021
Last Verified: June 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Additional relevant MeSH terms:
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Dental Plaque
Pulmonary Disease, Chronic Obstructive
Lung Diseases
Respiratory Tract Diseases
Lung Diseases, Obstructive
Dental Deposits
Tooth Diseases
Stomatognathic Diseases