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The influence of the use of Periodontal Guides on the predictability of the esthetic procedure of increasing the tooth exposed area through the Crown Lengthening Technique

The influence of the Guided Technique on the predictability of Esthetic Crown Lengthening procedures

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-68tfqj2
Enrollment
Unknown
Registered
2023-05-08
Start date
2020-08-13
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

Esthetics, Dental

Interventions

This is a randomized controlled clinical trial. Twenty participants will be randomly divided into two groups, one experimental and one control.Experimental group: 10 participants with altered passive
E06.323.115

Sponsors

Faculdade de Odontologia de Araraquara (Universidade Estadual Paulista)
Lead Sponsor
Faculdade de Odontologia de Araraquara (Universidade Estadual Paulista)
Collaborator

Eligibility

Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Complaint of gummy smile with altered passive eruption; age range between 18 and 40 years

Exclusion criteria

Exclusion criteria: Patients who underwent irradiation in the head and neck region; patients with immunosuppression and immunosuppression; patients who use or used anti-resorptive drugs or who alter bone metabolism; patients with poor oral hygiene; pregnant or lactating women; patients with uncontrolled diabetes; smokers and patients with unrealistic expectations

Design outcomes

Primary

MeasureTime frame
More predictable clinical crown lengthening results are expected when the periodontal surgical guide is used, and these data will be evaluate by overlaying the patient's digital files obtained before the surgical procedure (initial planning) and 3 months after the surgical procedure.

Secondary

MeasureTime frame
It is expected to find fewer complaints of pain from the participants when the dental guide is used. The analogical visual scale will be used for questionnaire by the participants who will be evaluated after 3, 7, 15 and 30 days of the experimented procedure

Countries

Brazil

Contacts

Public ContactMarcelo Gonçalves

Faculdade de Odontologia de Araraquara (Universidade Estadual Paulista)

marcelo.goncalves1970@unesp.br+55 16 33016311

Outcome results

None listed

Source: REBEC (via WHO ICTRP)