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Maxillary Vascular Canal Thickness and Sinus Augmentation Bleeding

Completed
Conditions
Bone Loss
Registration Number
NCT05710497
Lead Sponsor
Marmara University
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
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

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Total amount of intraoperative bleedingFrom beginning of surgery to end of surgery

After surgery, the total amount of intraoperative bleeding will be calculated in milliliters.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Marmara University School of Dentistry

🇹🇷

Istanbul, Turkey

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