Maxillary implant overdentures retained by use of bars or locator attachments: 5-year findings from a randomized controlled trial.

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON21557

Enrollment

Registered

2020-11-03

Start date

2020-11-03

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

Complaints of maxillary prosthesis

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Fully edentulous patients with complaints of their maxillary prosthesis, >18y/o, at least one year fully edentulous.

Exclusion criteria

Exclusion criteria: Previous preprosthetic surgery in maxilla, smoking, radiation therapy in head and neck region, medical contra-indications for surgery

Design outcomes

Primary

Measure	Time frame
Peri-implant bone loss	—

Secondary

Measure	Time frame
implant survival, changes in clinical (probing depth, modified bleeding index, gingiva index) parameters and patient satisfaction (validated questionnaires)	—

Contacts

Public ContactPieter Onclin

UMCG

p.onclin@umcg.nl0503611311

Outcome results