No registrations found.
ID
Source
Health condition
retentieverlies bovenprothese
atrofie van de bovenkaak
problems with retention of denture
atrophic maxilla
Sponsors and support
Intervention
Outcome measures
Primary outcome
Pain levels.
Secondary outcome
1. Donor site morbidity;
2. Intra oral morbidity;
3. Bone growth (histology).
Background summary
N/A
Study objective
Augmentation of the maxilla with calvarial bone has a lower complication rate than iliac crest bone.
Study design
First postoperative days, 2 weeks, 6 weeks, 12 weeks, 16 weeks, half year, one year, two years.
Intervention
Two standard treatments to augment the maxilla are compared.
Department of Oral Sugery
P.O. Box 30001
G.M. Raghoebar
Groningen 9700 RB
The Netherlands
+31(0)50 3613186
g.m.raghoebar@kchir.umcg.nl
Department of Oral Sugery
P.O. Box 30001
G.M. Raghoebar
Groningen 9700 RB
The Netherlands
+31(0)50 3613186
g.m.raghoebar@kchir.umcg.nl
Inclusion criteria
1. Edentulous patients;
2. Cannot wear an upper denture satisfactorily;
3. Have an atrophied maxilla with insufficient bone volume to support dental implants;
4. Written informed consent.
Exclusion criteria
1. Unable to be operated on due to severe health problems;
2. The use of intravenous bisphosphonates.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL3795 |
| NTR-old | NTR3968 |
| Other | : |
| ISRCTN | ISRCTN wordt niet meer aangevraagd. |