BOLERO: Prevalence of Mucosal Biofilm Formations in Adenoidectomy Specimens

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Completed
CT.gov ID
NCT01022944
Collaborator
Ministry of Health, France (Other)
113
1
2
22
5.1

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: With chronic middle ear effusion
  • Procedure: Without chronic middle ear effusion
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
113 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Prevalence of Mucosal Biofilm Formations in Adenoidectomy Specimens. A Case Control Study
Study Start Date :
Jul 1, 2010
Actual Primary Completion Date :
May 1, 2012
Actual Study Completion Date :
May 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Other: Group 2 :

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

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

Other: Group 1

Children with chronic middle ear effusion having adenoidectomy.

Procedure: With chronic middle ear effusion
Children with chronic middle ear effusion having adenoidectomy.

Outcome Measures

Primary Outcome Measures

  1. Prevalence of mucosal biofilm formations in adenoidectomy specimens analyzed using Confocal Laser Scanning Microscopy with double staining [at 2 years]

Secondary Outcome Measures

  1. To build up a tissue bank of human tissue from adenoids and the middle ear for further bacterial identification [during the study]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Months to 10 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hôpital ROBERT DEBRE - ORL Pédiatrique Paris France 75020

Sponsors and Collaborators

  • Assistance Publique - Hôpitaux de Paris
  • Ministry of Health, France

Investigators

  • Principal Investigator: Romain KANIA, MD, Assistance Publique - Hôpitaux de Paris

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT01022944
Other Study ID Numbers:
  • P080605
First Posted:
Dec 1, 2009
Last Update Posted:
Jun 1, 2021
Last Verified:
May 1, 2021
Keywords provided by Assistance Publique - Hôpitaux de Paris
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 1, 2021