Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
Healthy Volunteers
ID02137824

A Modified Minimally Invasive Technique for Sinus Floor Elevation in Patients with Residual Bone Height of 3-6 mm

Led by Medical University of Vienna · Updated on 2023-03-15

12

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to develop and test a modified minimally invasive surgical technique for sinus floor augmentation in patients with a residual bone height of 3 to 6 millimeters. The goal is to create a reliable implant bed of at least 10 millimeters in height after a healing period of 3 to 5 months. The study also seeks to reduce patient stress compared to traditional methods. Participants will undergo the sinus floor elevation procedure, which is being evaluated to improve outcomes and comfort. This surgical technique is studied on a pilot group of 12 patients, with no placebo or comparative treatments involved. The procedure targets the maxillary sinus area to enhance bone structure for dental implant placement. During the study, participants will be monitored to measure the height of bone augmentation after 4 to 5 months of healing. The research team will assess the surgical results and patient recovery, including any side effects or complications. The total duration includes the surgery followed by the healing and evaluation period to determine the procedure's effectiveness and patient impact.

CONDITIONS

Brief Title

A Modified Sinus Floor Elevation Technique - a Pilot Study on 12 Patients

Who Can Participate

Age: 18Years - 100Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 100 years
  • Residual bone height of 3 to 6 millimeters
  • Residual bone width greater than 4 millimeters
Not Eligible

You will not qualify if you...

  • Untreated periodontal disease
  • Smoking more than 5 cigarettes per day
  • Acute or chronic sinusitis

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

Duration - Single procedure with immediate recovery period

Participants undergo a modified sinus floor elevation procedure followed by immediate post-operative care.

1 procedure visit (in-person)

Post-operative Follow-up

Duration - 4 to 5 months

Participants are followed up to assess healing and augmentation height after surgery.

1 to 2 follow-up visits

Trial Site Locations

Total: 1 location

1

Bernhard Gottlieb School of Dentistry, Medical University of Vienna

Vienna, Austria, 1090

Actively Recruiting

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Research Team

K

Kristina Bertl, PD, DMD, MSc

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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