Influence of Dental Scaling on the adaptation of Complete Dentures

Influence of prior Supragingival Scaling on tissue healing and adaptation of Immediate Complete Dentures

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

REBEC

Registry ID

RBR-879qjjx

Enrollment

Registered

2026-03-25

Start date

2026-05-01

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

Periodontitis Tooth loss

Interventions

This will be a single-blind,/ randomized trial in a parallel-model study with two arms. Thirty patients with an indication for extraction of all teeth due to periodontal disease will be randomly distr

Eligibility

Age

30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Indication for extraction of all teeth due to periodontal disease in the maxilla or mandible; Age between 30 and 70 years; Need for total rehabilitation with a prosthesis; Sufficient health conditions to undergo surgical procedure (ASA I and ASA II); Sufficient cognitive capacity to understand the procedures to be performed and the Informed Consent Form

Exclusion criteria

Exclusion criteria: Smokers who consume more than 20 cigarettes daily; Those using medications that alter bone metabolism; Pregnant and breastfeeding women; History of head and neck radiotherapy; Insufficient cognitive function to understand the research protocol.

Design outcomes

Primary

Measure	Time frame
The primary variable in this study will be the Mechanical, Aesthetic/Anatomical, Pathophysiologic (MAPS) healing index. It is expected that the intervention group will show better index variables, with scores 1 point higher than the score obtained in the control group	—

Secondary

Measure	Time frame
The number of prosthesis relinings will be a secondary outcome of this study. It is expected that the Intervention group will have 10% less need for prosthesis relinings during the follow-up phase of this study compared to the control group;Patient-centered outcomes (pain, discomfort, burning mouth syndrome, swallowing, adaptation to the temporary prosthesis), which will be assessed using the VAS scale, will be secondary outcomes in this study. It is expected that the Intervention group will show a 1-point decrease on the visual analogic scale (VAS) scale during the follow-up phase of this study compared to the control group;The presence of residual bone spicules will be a secondary outcome of this study. It is expected that the Intervention group will present 10% fewer occurrences of bone spicules during the follow-up phase of this study compared to the control group	—

Measure

Time frame

The number of prosthesis relinings will be a secondary outcome of this study. It is expected that the Intervention group will have 10% less need for prosthesis relinings during the follow-up phase of this study compared to the control group;Patient-centered outcomes (pain, discomfort, burning mouth syndrome, swallowing, adaptation to the temporary prosthesis), which will be assessed using the VAS scale, will be secondary outcomes in this study. It is expected that the Intervention group will show a 1-point decrease on the visual analogic scale (VAS) scale during the follow-up phase of this study compared to the control group;The presence of residual bone spicules will be a secondary outcome of this study. It is expected that the Intervention group will present 10% fewer occurrences of bone spicules during the follow-up phase of this study compared to the control group

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Countries

Contacts

Public ContactGuilherme Oliveira

Universidade Federal de Uberlândia

guilherme.lopesoliveira@ufu.br+55(34)32258132

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Apr 4, 2026