Skip to content

Single implant-retained removable mandibular complete denture: non randomized controlled clinical study

Single implant-retained mandibular overdenture: non-randomized controlled clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3hvsy5
Enrollment
Unknown
Registered
2020-06-24
Start date
2020-09-01
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

Interventions

A total of 50 patients will be rehabilitated with bimaxillary complete dentures and will be waited for 3 months to assess the adaptation/use of the new mandibular complete dentures. After this follow
n = 25) and PTI group (not adapted to mandibular complete denture
n = 25). At that time, data collections will be carried out regarding satisfaction with the mandibular complete denture, masticatory performance, quality of life related to oral health, technical qual
Procedure/surgery
Q65.070

Sponsors

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

Eligibility

Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patients must be 60 years or older, good general health status, absence of intraoral lesions, and changes in the perioral muscles detected by palpation. Patients whose implants can be placed in the mandible without bone graft (minimum bone height of 8 mm), user of the upper conventional complete denture, use or nonuse the lower complete denture, and need new conventional complete dentures.

Exclusion criteria

Exclusion criteria: Edentulous with local bone deficiency, systemic disease that prevents implant placement, history of chemotherapy or radiotherapy, users of bisphosphonate drugs.

Design outcomes

Primary

MeasureTime frame
The rehabilitation procedure of single implant installation and conversion to overdenture will promote greater adaptation and acceptance of patients to the mandibular total rehabilitation, however, this adaptation will be superior in patients not adapted to the conventional mandibular complete denture, which will be evaluated based on satisfaction with the new complete dentures, and the impact of the quality of life on oral health.

Secondary

MeasureTime frame
The masticatory performance, verified by the objective method of tamises, will be reduced in patients not adapted to mandibular prostheses 3 months after the conversion of the total prosthesis into mandibular overdenture. The quality of life in oral health, measured through OHIP, will have a greater positive impact on individuals not adapted to the mandibular prosthesis, contributing to greater satisfaction with overdenture for the performance of masticatory, phonetics, and social relationships.

Countries

Brazil

Contacts

Public ContactAretha Verissimo

Universidade Federal do Rio Grande do Norte

aretha.heitor@gmail.com+55 (84) 988141514

Outcome results

None listed

Source: REBEC (via WHO ICTRP)