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Implant-supported three-unit fixed dental prosthesis using coded healing abutments and fabricated by digital workflow: a 5-year prospective case series study

Implant-supported three-unit fixed dental prosthesis using coded healing abutments and fabricated by digital workflow: a 5-year prospective case series study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21760
Enrollment
60
Registered
2020-02-06
Start date
2020-05-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

missing teeth in the posterior region

Interventions

Implant supported 3-unit fixed dental prosthesis

Sponsors

none
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: This prospective case series study considered all consecutive patients were eligible to participate, if they had at least three adjacent missing teeth in the posterior region of the mandible or maxilla and were treated with a 3-unit FDP on 2 implants. All patients were screened using clinical and radiographic examinations to determine if they met all of the following inclusion criteria: - over 18 years of age and capable of understanding and giving informed consent; - sufficient horizontal and vertical space to place a three-unit FDP; - sufficient bone levels at the proposed implant sites to place implants with a length of at least 8.5mm and a width of 4mm; - the presence of natural antagonistic teeth or a prosthetic construction.

Exclusion criteria

Exclusion criteria: Any of the following was regarded as a criterion for exclusion from the study: - uncontrolled pathological processes in the oral cavity; - known or suspected current malignancy; - history of radiation therapy in the head and neck region; - history of chemotherapy within 5 years prior to surgery; - systemic or local disease, condition or medication that could compromise postoperative healing and/or osseointegration; - is a smoker (and intends to continue); - regular alcohol and/or drug use.

Design outcomes

Primary

MeasureTime frame
Survival of the implants and reconstruction

Secondary

MeasureTime frame
Success of the prosthesis, condition of the surrounding hard and soft tissue

Contacts

Public ContactChristiaan Pol

University Medical Center Groningen

c.w.p.pol@umcg.nl0503616276

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)