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Gingival assessment around the teeth in patients using partial dentures

Periodontal evaluation in removable partial dentures wearers

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-97v6f5
Enrollment
Unknown
Registered
2015-10-08
Start date
2014-05-25
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Stomatognathic diseases, periodontal diseases

Interventions

80 patients edentulous upper and partially edentulous in the lower arch, denture wearers upper and lower partial denture, of both sexes, after the diagnosis of periodontal disease patients will be tre
Procedure/surgery
E06.721.189.350

Sponsors

Universidade Federal do Rio Grande do Norte
Lead Sponsor
Universidade Federal do Rio Grande do Norte
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Minimum age 18 years. Both genders. Have been met and rehabilitated with maxillary denture and lower removable partial Kennedy Class I. Treated at the service of the Faculty of Dentistry of the Federal University of Rio Grande do Norte.

Exclusion criteria

Exclusion criteria: Over 80 years. Weakened state of health.

Design outcomes

Primary

MeasureTime frame
Increased clinical insertion after 6-month evaluation verified by periodontal probing after observation of decrease in periodontal parameters of probing depth and gingival retraction after intervention, at the end of treatment.

Secondary

MeasureTime frame
Improving clinical periodontal parameters verified by clinical periodontal evaluation from the constação improvement in periodontal status of abutment teeth. Decrease in the visible plaque index verified by clinical assessment based on the statement of the decreased amount of biofilm on the teeth retainers of the prosthesis in relation the amount observed at the first assessment. Decreased bleeding on probing checked with probing examination from the evidence of the absence of bleeding after probing.

Countries

Brazil

Contacts

Public ContactBruno de Vasconcelos Gurgel

Programa de Pós-graduação em Saúde Coletiva

bcgurgel@yahoo.com.br+55 (84) 32154100

Outcome results

None listed

Source: REBEC (via WHO ICTRP)