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Single tooth implants in the posterior maxilla and mandible: a prospective study on clinical performance of NobelBiocare Implants restored with screw-retained zirconia crowns; a 5-years evaluation

Single tooth implants in the posterior maxilla and mandible: a prospective study on clinical performance of NobelBiocare Implants restored with screw-retained zirconia crowns; a 5-years evaluation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON24338
Enrollment
30
Registered
2021-10-29
Start date
2021-12-01
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

5-years ago the patient had a missing posterior tooth

Interventions

Dental implant with a full-zirconia restoration

Sponsors

University Medical Center Groningen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Patients referred to the department of Oral and Maxillofacial Surgery 5 years ago and treated with a dental implant and a screw-retained implant-supported zirconia restoration because of having a missing tooth in the posterior region. At the time of treatment: • The patient was 18 years or older; • The missing tooth was a premolar or molar in maxilla or mandible; • Sufficient healthy and vital bone to insert a dental implant with a minimum length of 8 mm and at least 4.0 mm in diameter with initial stability > 45 Ncm • The implant site was free from infection; • Adequate oral hygiene (modified plaque index and modified sulcus bleeding index = 1); • Sufficient mesio-distal, bucco-lingual, and interocclusal space for placement of an anatomic restoration; • The patient was capable of understanding and giving informed consent.

Exclusion criteria

Exclusion criteria: • Medical and general contraindications for the surgical procedures; • Presence of an active and uncontrolled periodontal disease; • Bruxism; • Smoking • A history of local radiotherapy to the head and neck region.

Design outcomes

Primary

MeasureTime frame
Change in marginal peri-implant bone level 5 years after placing the definitive restoration.

Secondary

MeasureTime frame
Implant and restoration survival, peri-implant mucosa health and patients’ satisfaction using a questionnaire.

Contacts

Public ContactHenny J.A. Meijer

University Medical Center Groningen

h.j.a.meijer@umcg.nl+31503613840

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)