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Prevalence of Mucosal Biofilm Formations in Adenoidectomy Specimens (BOLERO)

Primary Purpose

Chronic Serous Otitis Media, Simple or Unspecified

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
With chronic middle ear effusion
Without chronic middle ear effusion
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Chronic Serous Otitis Media, Simple or Unspecified focused on measuring Serous otitis media, Biofilm, Adenoidectomy, Chronic otitis media

Eligibility Criteria

18 Months - 10 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Group 1 and 2

    • obtained informed consent by both parents and child (if possible),
    • age > 18 months and <10 years
    • chronic serous otitis media lasting more than 3 months (group 1).
  • Group 1 only:

    • chronic secretory otitis media
  • Group 2 only:

    • hypertrophia adenoid vegetations without sinusal oropharyngeal infections

Exclusion criteria:

  • No informed consent
  • age < 18 months or > 10 years
  • Eustachian tube dysfunction
  • Immunodeficiency
  • Tumor

Sites / Locations

  • Hôpital ROBERT DEBRE - ORL Pédiatrique

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Group 2 :

Group 1

Arm Description

Children without chronic middle ear effusion as a control group having adenoids removed for chronic obstruction.

Children with chronic middle ear effusion having adenoidectomy.

Outcomes

Primary Outcome Measures

Prevalence of mucosal biofilm formations in adenoidectomy specimens analyzed using Confocal Laser Scanning Microscopy with double staining

Secondary Outcome Measures

To build up a tissue bank of human tissue from adenoids and the middle ear for further bacterial identification

Full Information

First Posted
September 30, 2009
Last Updated
May 27, 2021
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Ministry of Health, France
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1. Study Identification

Unique Protocol Identification Number
NCT01022944
Brief Title
Prevalence of Mucosal Biofilm Formations in Adenoidectomy Specimens
Acronym
BOLERO
Official Title
Prevalence of Mucosal Biofilm Formations in Adenoidectomy Specimens. A Case Control Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
May 2012 (Actual)
Study Completion Date
May 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Ministry of Health, France

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Rationale: Bacterial biofilms are defined as an assemblage of bacterial cells enclosed in a self-produced glycocalyx matrix. Adherence on surfaces, and resistance to both antibiotic treatments and host defenses are ones of the major clinical features of bacterial biofilms. Hence, biofilm formations represent a serious clinical problem: they persist in human tissues and play a role in a large number of chronic and resistant infections. It has been estimated that more than 65% of all human bacterial infections involve biofilms. Recently, the investigators have demonstrated the presence of mucosal bacterial biofilms in adenoid tissues removed during routine adenoidectomy. Bacterial biofilms were visualized using Confocal Laser Scanning Microscopy (CLSM) with a technique of double staining showing both the bacterial cells and the glycocalyx matrix. Although this study clearly established that adenoids tissues can harbour mucosal biofilms, the prevalence of 54% the investigators found suggested that some groups of children may contain more biofilm formations than others. In an effort to relate the findings of mucosal biofilm with the clinical presentation, the investigators have designed the present work to compare the prevalence of mucosal biofilms in adenoidectomy specimens in two groups: one group of children with chronic otitis media (COM) with effusion versus another group of children without any COM, having adenoids removed for chronic obstruction.
Detailed Description
The aim of this case-control study is to compare the prevalence of biofilms formations in adenoid tissues of children with COM versus a control group without any COM. Design: This is a monocentric, prospective, unrandomized case-control study comparing the prevalence of biofilm formations in adenoid tissues of two groups. Clinical research study without direct medical benefit: during routine adenoidectomy, specimens are not used and thrown away. This study do not modify the common management of included children. Number of subjects required: A considered approach of simple size calculation have been made using a method proposed by MIETINEN for Mc NEMAR Chi2 test. Simple size N=104 will allow 80% power to detect different of 20% (absolute), considering a total percentage of discordance pair at 30 %. Expected results: a higher prevalence (30% estimation) of biofilm formations in group 1 in comparison with that in group 2 would be the first clinical research study bringing understanding of the role of adenoid tissues by harboring mucosal biofilms in otitis prone children.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Serous Otitis Media, Simple or Unspecified
Keywords
Serous otitis media, Biofilm, Adenoidectomy, Chronic otitis media

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
113 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 2 :
Arm Type
Other
Arm Description
Children without chronic middle ear effusion as a control group having adenoids removed for chronic obstruction.
Arm Title
Group 1
Arm Type
Other
Arm Description
Children with chronic middle ear effusion having adenoidectomy.
Intervention Type
Procedure
Intervention Name(s)
With chronic middle ear effusion
Intervention Description
Children with chronic middle ear effusion having adenoidectomy.
Intervention Type
Procedure
Intervention Name(s)
Without chronic middle ear effusion
Intervention Description
Children without chronic middle ear effusion as a control group having adenoids removed for chronic obstruction.
Primary Outcome Measure Information:
Title
Prevalence of mucosal biofilm formations in adenoidectomy specimens analyzed using Confocal Laser Scanning Microscopy with double staining
Time Frame
at 2 years
Secondary Outcome Measure Information:
Title
To build up a tissue bank of human tissue from adenoids and the middle ear for further bacterial identification
Time Frame
during the study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Months
Maximum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Group 1 and 2 obtained informed consent by both parents and child (if possible), age > 18 months and <10 years chronic serous otitis media lasting more than 3 months (group 1). Group 1 only: chronic secretory otitis media Group 2 only: hypertrophia adenoid vegetations without sinusal oropharyngeal infections Exclusion criteria: No informed consent age < 18 months or > 10 years Eustachian tube dysfunction Immunodeficiency Tumor
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Romain KANIA, MD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital ROBERT DEBRE - ORL Pédiatrique
City
Paris
ZIP/Postal Code
75020
Country
France

12. IPD Sharing Statement

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Prevalence of Mucosal Biofilm Formations in Adenoidectomy Specimens

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