Maxilla augmentation with calvarial bone or iliac crest bone: a compariso

Completed

• Conditions: atrofy maxilla; resorbed maxilla; 10005944

• Registration Number: NL-OMON41214
• Lead Sponsor: niversitair Medisch Centrum Groningen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 20

Inclusion Criteria

- edentulous patients that
- cannot wear an upper denture satisfactorily
- have an atrophied maxilla with insufficient bone volume to support dental implants
- written informed consent

Exclusion Criteria

- Unable to be operated on due to severe health problems
- The use of intravenous bisphosphonates
- Pregnant or breast-feeding
- Allergic reaction in past toTetracycline

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Bone volume (%) of calvarial and iliac crest bone at time of harvesting and at<br /><br>time of 4 months healing</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Bone formation of calvarial and iliac crest graft at 4 months healing<br /><br>(micrometers per day)<br /><br><br /><br>Third outcome: average pain and complication rate of both groups</p><br>