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Clinical Trials/DRKS00003730
DRKS00003730
Completed
未知

Single dental implant retained mandibular complete dentures – influence of the loading protocol - SDI-Study

niversitätsklinikum Schleswig-Holstein Campus Kiel0 sites169 target enrollmentAugust 23, 2012
ConditionsEdentoulism

Overview

Phase
未知
Intervention
Not specified
Conditions
Edentoulism
Sponsor
niversitätsklinikum Schleswig-Holstein Campus Kiel
Enrollment
169
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 23, 2012
End Date
September 25, 2019
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversitätsklinikum Schleswig-Holstein Campus Kiel

Eligibility Criteria

Inclusion Criteria

  • Edentulous patients in the age of 60\-89 years without contraindication for implantation and sufficient bone in the anterior mandible to place an implant without augmentation procedures.
  • \- Residual bone height is 11 to 20 mm (Type II and III according to McGarry et al.) at the least vertical height of the mandible and vertical bone height in the midline of the mandible is at least 13 mm.
  • \- Despite technically acceptable complete dentures in mandible and maxilla the patient is unsatisfied with the retention and/or stability of the mandibular denture while the denture in the maxilla has adequate retention and stability.
  • \- To allow adaptation existing dentures have been worn at least for 3 months. Dentures must have a bilaterally balanced occlusal scheme.

Exclusion Criteria

  • \- Edentulous patients in the age of 60\-89 years with contraindication for implantation in the mandible caused by systematic diseases or local bone deficits.
  • \- Patients who are satisfied with the retention of their mandibular denture or who are unsatisfied with the retention and/or stability of their denture in the maxilla.
  • \- Subjects with Symptom Check list\-90\- R(evised) (SCL\-90\-R, German version) index T\-scores of 70 or greater or with two symptom scale scores of 70 or greater will be excluded from the study.

Outcomes

Primary Outcomes

Not specified

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