Clinical Study of Oral Endosseous Titanium Implants in Edentulous Subjects
Completed
Conditions studied: Ectodermal Dysplasia, Jaw, Edentulous
In brief
The amendment to Clinical Protocol 86-D-0015, clinical study of Oral Endosseous Titanium Implants in Edentulous subjects, and patients with Ectodermal Dysplasia is to allow the Investigators to determine: (1) If placement of Endosseous Titanium Implants in pre-adolescent patients (age 7 to 10) will influence the growth and development of the craniomandibular complex. (2) The final position of the implant, the ability to fabricate prosthesis. (3) Body image, diet and perceived ease of chewing selected foods. Selection of patients for participation in the study will be based on the number of congenitally missing teeth associated with Ectodermal Dysplasia. At least 16 permanent teeth must be congenitally missing. A total of 30 patients will be included. A consent to participate in this study will be obtained from each patient: 18 \& older - consent signed by patient 13-17 years - consent signed by parent, assent signed by patient 7-10 years - consent by parent, assent signed by child if capable of understanding or note on chart describing procedure used to obtain the child's assent to the study
Key facts
- Study ID
- NCT00001211
- Run by
- National Institute of Dental and Craniofacial Research (NIDCR)
- People needed
- 160
- Starts
- 1986-01-01
- Expected to finish
- 2000-12-01
- Last updated by the study team
- 2008-03-04
Who can join
Age: any. Sex: any. Healthy volunteers: accepted.
Where it is running
- National Institute of Dental And Craniofacial Research (NIDCR) — Bethesda, Maryland, United States
Full record on ClinicalTrials.gov
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