- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02833337
Morphological Pattern of the Atrophic Posterior Maxillae
Overcoming the vertical and horizontal bone deficiency in the posterior maxillae are considered as the most challenging scenarios for implant-supported oral rehabilitation in modern implant dentistry. Therefore, a comprehensive and precise understanding of such anatomical structures are needed to avoid potential complications that ultimately might jeopardize the treatment outcome.
Cone-beam computerized tomography (CBCT) offers some advantages to conventional CT-scan such as lower-dose radiation with high isotropic spatial resolution and cost. Therefore, it offers a viable and reliable tool to study anatomical structures such as the posterior atrophic maxillae
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Badajoz, Spain, 06001
- Florencio Monje Gil
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Images were included if:
- Pristine maxillary posterior atrophic ridges (between premolars and molars) as a result of missing single or multiple teeth for over than 12 months.
- Residual ridge height (RH) was < 10 mm.
- Presence of teeth adjacent to or opposing the edentulous area so the location of the edentulous ridges corresponding to the tooth site could be identified.
- The maxillary sinus to be measured was visible from its floor to at least 15 mm from the alveolar crest of the edentulous ridge.
Images were excluded if:
- Images were unclear or incomplete due to scattering or other reasons
- Edentulous ridge height was more than 10 mm
- Ridge preservation/augmentation simultaneous/delayed to tooth extractions
- Grafted maxillary sinus for implant-supported prosthesis
- The location of the edentulous ridge cannot be determined
- Implants or other prosthetic device restoring the posterior ridge
- Presence of sinus pathology that made the measurement impossible
- The outline of the edentulous ridge cannot be identified due to low 'grey scale' density
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lateral Wall Thickness
Time Frame: One month
|
Thickness measured in mm of the lateral aspect of the maxillary sinus
|
One month
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 52/2012
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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