Skip to content

Morphological Pattern of the Atrophic Posterior Maxillae

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02833337
Enrollment
180
Registered
2016-07-14
Start date
2016-07-31
Completion date
2016-09-30
Last updated
2020-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bone Deficiency, Posterior Maxillae

Keywords

Bone, Maxilla, Cone-Beam Computed Tomography, Regeneration

Brief 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

Interventions

RADIATIONCone-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.

Sponsors

Center of Implantology, Oral and Maxillofacial Surgery, Badajoz, Spain
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Lateral Wall ThicknessOne monthThickness measured in mm of the lateral aspect of the maxillary sinus

Countries

Spain

Participant flow

Participants by arm

ArmCount
Consecutive Individuals
Consecutive individuals explored via cone-beam computed tomography to evaluate the anatomical features
180
Total180

Baseline characteristics

CharacteristicConsecutive Individuals
Age, Categorical
<=18 years
20 Participants
Age, Categorical
>=65 years
50 Participants
Age, Categorical
Between 18 and 65 years
110 Participants
Age, Continuous57 years
STANDARD_DEVIATION 9
Region of Enrollment
Spain
180 participants
Sex: Female, Male
Female
80 Participants
Sex: Female, Male
Male
100 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 0
serious
Total, serious adverse events
0 / 0

Outcome results

Primary

Lateral Wall Thickness

Thickness measured in mm of the lateral aspect of the maxillary sinus

Time frame: One month

ArmMeasureValue (MEAN)Dispersion
Consecutive IndividualsLateral Wall Thickness161 mmStandard Deviation 11

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026