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Clinical Study of the Presence of Trichomonas Tenax and Entamoeba Gingivalis in Patients With Periodontitis

Preliminary Clinical Study of the Presence of Trichomonas Tenax and Entamoeba Gingivalis in Patients With Periodontitis Consulting to CHU of Nancy, in Periodontal Department.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03178838
Acronym
Paro-Proto 2
Enrollment
50
Registered
2017-06-07
Start date
2013-12-03
Completion date
2014-11-11
Last updated
2017-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Periodontitis, Adult

Brief summary

The buccal cavity presents microorganismes whose the number and composition vary with oral hygiene and medical context (pathologies and associated drug therapies) of the patient. More than 1200 bacterial species have been identified, and among them, 400 are inhabitants of the sub-gingival biofilm. Among all these microorganismes, only 20 species participate to the etiopathogenesis of periodontal diseases.Some are recognised as major periodontopathogens other play unclear role in this pathology. They belong respectively to the red and orange complex of Socransky et al. (1998). Other microorganismes such as virures, yeasts and protozoans could potentially impact the emergence and development of periodontal diseases. The presence of protozoans in periodontitis have been investigated in this study.

Interventions

None listed

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults \> 18 years-old * Consulting in periodontal department of CHU, Nancy * Patient with moderate to severe periodontitis * At least 2 periodontal sites with PPD≥ 4mm and One healthy site * No scaling root planning in the last 6 months * Patients insured under the French social security system

Exclusion criteria

* Pregnant patients * Patients with antibiotic therapy, and/or all medecines which could modify the buccal microbiota in the last 6 months * Tooth with endodontic periapical lesion * Patients having a scaling root planning in the last 6 months * Patient with guardianship

Design outcomes

Primary

MeasureTime frame
Presence of protozoansbaseline

Secondary

MeasureTime frame
Periodontal pocket depth (mm)baseline
Clinical attachment loss (mm)baseline
Plaque and gingival indexbaseline
Mobility of the tooth (Yes/No)baseline
Presence of bleeding on probing (Yes/No)baseline

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026