Skip to content

Maxillary Vascular Canal Thickness and Sinus Augmentation Bleeding

Assessing the Correlation of Maxillary Vascular Canal Thickness With Intraoperative Bleeding During Open Sinus Floor Augmentation: A Volumetric Tomography Study.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05710497
Enrollment
20
Registered
2023-02-02
Start date
2023-03-01
Completion date
2023-11-07
Last updated
2023-11-08

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

Conditions

Bone Loss

Keywords

Maxillary Sinus Floor Augmentation, Volumetric Computed Tomography, Intra-operative bleeding

Brief summary

This study aims to evaluate the relationship between the maxillary intra-osseous vascular canal thickness as measured by volumetric tomography and the amount of intra-operative bleeding during open sinus floor augmentation. A sample of patients will be selected, and their maxillary intra-osseous vascular canal thickness will be measured using volumetric tomography. Intraoperative bleeding will be recorded during open sinus floor augmentation. The data will be analyzed to determine if there is a correlation between the thickness of the maxillary intra-osseous vascular canal and intraoperative bleeding.

Interventions

None listed

Sponsors

Marmara University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years

Inclusion criteria

* Maxillary partial or total edentulism, including premolar/molar regions * Medically healthy * 2 to 5 mm residual bone height * Sufficient bone width to place a standard dental implant (diameter \>4mm) * Age: 18-65 years * Patients who volunteered to participate in the study and signed written informed consent

Exclusion criteria

* Maxillary sinusitis * Acute myocardial infarction in the last 12 months * Use of any medication that may inhibit bone healing * History of radiotherapy in the head and neck region * Presence of psychiatric problems * Smoking more than 10 cigarettes a day * Alcoholism * Chronic drug use

Design outcomes

Primary

MeasureTime frameDescription
Total amount of intraoperative bleedingFrom beginning of surgery to end of surgeryAfter surgery, the total amount of intraoperative bleeding will be calculated in milliliters.

Countries

Turkey (Türkiye)

Outcome results

None listed

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