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Maxillary Vascular Canal Thickness and Sinus Augmentation Bleeding

M

Marmara University

Status

Completed

Conditions

Bone Loss

Study type

Observational

Funder types

Other

Identifiers

NCT05710497
MUDHF_FB_004

Details and patient eligibility

About

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.

Enrollment

20 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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