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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02833337
Other study ID # 52/2012
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 2016
Est. completion date September 2016

Study information

Verified date August 2020
Source Center of Implantology, Oral and Maxillofacial Surgery, Badajoz, Spain
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 180
Est. completion date September 2016
Est. primary completion date September 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility - Images were included if:

1. Pristine maxillary posterior atrophic ridges (between premolars and molars) as a result of missing single or multiple teeth for over than 12 months.

2. Residual ridge height (RH) was < 10 mm.

3. 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.

4. 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:

1. Images were unclear or incomplete due to scattering or other reasons

2. Edentulous ridge height was more than 10 mm

3. Ridge preservation/augmentation simultaneous/delayed to tooth extractions

4. Grafted maxillary sinus for implant-supported prosthesis

5. The location of the edentulous ridge cannot be determined

6. Implants or other prosthetic device restoring the posterior ridge

7. Presence of sinus pathology that made the measurement impossible

8. The outline of the edentulous ridge cannot be identified due to low 'grey scale' density

Study Design


Related Conditions & MeSH terms

  • Bone Deficiency, Posterior Maxillae

Intervention

Radiation:
Cone-beam computed topography
This study used a retrospective database of preexisting data that included patients treated as part of routine periodontal and oral surgery therapy for each patient's needs. All the patients signed an inform consent approving using their radiographic data for research purposes.

Locations

Country Name City State
Spain Florencio Monje Gil Badajoz

Sponsors (1)

Lead Sponsor Collaborator
Center of Implantology, Oral and Maxillofacial Surgery, Badajoz, Spain

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Lateral Wall Thickness Thickness measured in mm of the lateral aspect of the maxillary sinus One month