Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT07017413

Predictors For Transosseous Maxillary Sinus Lift Complications

Led by University of Baghdad · Updated on 2025-06-12

60

Participants Needed

2

Research Sites

53 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This prospective cohort study aims to identify clinical and anatomical predictors for complications following transosseous maxillary sinus lift procedures using the Versah (Densah burs) technique. The study focuses on patients undergoing transcrestal sinus floor elevation without a lateral window, with or without simultaneous dental implant placement. Variables such as residual bone height, sinus membrane thickness, bone density, and patient-related factors are being evaluated. The objective is to enhance risk stratification and optimize treatment planning for transosseous sinus augmentation.

CONDITIONS

Official Title

Predictors For Transosseous Maxillary Sinus Lift Complications

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients requiring dental implants in the posterior maxilla with a residual bone height of less than 6 mm
  • Good general health and absence of systemic conditions affecting bone healing, such as uncontrolled diabetes or osteoporosis
  • No history of chronic sinusitis or other significant sinus diseases
Not Eligible

You will not qualify if you...

  • Severe periodontal disease
  • Residual bone height greater than 6 mm
  • History of previous sinus lift procedures or other maxillofacial surgeries
  • Smokers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

College of Dentistry , University of Baghdad

Baghdad, Bab Almodaum, Iraq, 1214

Actively Recruiting

2

Planto clinic

Baghdad, Mansour, Iraq, 1456

Actively Recruiting

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Research Team

M

Mustafa Al-Jamal, BDS, MSc, PhD

CONTACT

A

Ahmed Quisi, BDS. FIBMS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

1

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