Skip to content

How the recovery of front teeth with implants by the unified health system works: evaluating efficiency in the dental trauma clinic

Implant rehabilitation protocols for anterior tooth loss in SUS patients: analysis of effectiveness associated with the dentoalveolar trauma clinic - SUS Unified Health System

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-8ckxj5g
Enrollment
Unknown
Registered
2024-11-27
Start date
2025-01-05
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

Dental Implants

Interventions

This is a prospective clinical trial that will evaluate the 1-year outcomes of treatment with single-unit implant-supported prostheses in the anterior maxillary region of young adult patients with ant
2) implant placement protocol: immediate or delayed
3) need for guided bone regeneration: yes or no
4) implant loading: immediate or delayed.

Sponsors

Faculdade de Odontologia - Universidade Federal de Uberlândia
Lead Sponsor
Faculdade de Odontologia da Universidade Federal de Uberlândia
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patient level: age greater than 18 and less than or equal to 60 years old; both genders; anterior tooth loss (single or multiple) or tooth with indicated extraction, assessed as sufficient for surgical planning; willingness to participate and sign informed consent. Implant site level: healed anterior edentulous space (at least 8 weeks since extraction), or tooth indicated for extraction due to fracture; coronary destruction with unfeasibility of recovery; minimum ridge dimensions of 5.4 mm (width) by 12 mm (height) in the anterior region of the maxilla, allowing the installation of implants with a regular or narrow diameter and a minimum length of 10 mm

Exclusion criteria

Exclusion criteria: Exclusion criteria at the patient level: inability to perform adequate oral hygiene or post operative care; inability to provide written informed consent and/or compliance with the study protocol; any contraindication to oral surgery, such as (but not limited to) uncontrolled diabetes, immunosuppression, radiation, chemotherapy or anti resorptive medication such as bisphosphonates; presence of multiple posterior edentulous spaces with an indication for extensive oral rehabilitation; heavy smoking with more than 20 cigarettes/day

Design outcomes

Primary

MeasureTime frame
Evaluation of the survival/success rates of implants and prostheses

Secondary

MeasureTime frame
Analyze the costs associated with each intervention approach and their relationship to clinical outcomes and patient quality of life, particularly in the context of the public healthcare system

Countries

Brazil

Contacts

Public ContactPriscilla Soares

Faculdade de Odontologia da Universidade Federal de Uberlândia

pbfsoares@yahoo.com.br+55-34-32258106

Outcome results

None listed

Source: REBEC (via WHO ICTRP)