Skip to content

Minimally Invasive Lateral Approach for Sinus Augmentation: a Split-mouth Randomized Clinical Trial.

Minimally Invasive Lateral Approach for Sinus Augmentation: a Split-mouth Randomized Clinical Trial.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02117882
Enrollment
15
Registered
2014-04-21
Start date
2013-01-31
Completion date
2014-04-30
Last updated
2014-04-21

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

Conditions

Bone Involvement in Diseases Classified Elsewhere

Keywords

lateral approach, bone augmentation , sinus floor elevation

Brief summary

It is assumed that the minimally invasive lateral approach and the traditional lateral sinus lift procedure will result in better outcomes in terms of height of augmented bone. It is also assumed that the minimally invasive lateral approach will reduce surgical complications and patient's discomfort in comparison with a traditional lateral sinus lift procedure.

Detailed description

16 patients edentulous in maxillary posterior area will be treated with a bilateral sinus lift procedure. Once a patient will be enrolled in the study impressions will be taken. After the wax-up, a radiographic stent will be prepared. Special attention will be given to position radio-opaque references in the positions where the implants will be inserted according to a prosthodontic guided insertion. Pre-surgical CT scan will be executed after placing the stent in its proper position in patient's mouth. After that, if no surgical contra-indications will be detected at CT evaluation, patients will be enrolled for surgical interventions.

Interventions

None listed

Sponsors

University of Firenze and Siena, Napoli, Italy
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* \- patient edentulous in the maxillary posterior area on both left and right side( not completely edentulous). * \- residual bone height in the maxillary premolar and molar region less than 4mm.

Exclusion criteria

* \- history of systemic diseases that would contraindicate surgical treatment

Design outcomes

Primary

MeasureTime frame
height of augmented bone6 months

Secondary

MeasureTime frame
post surgical patient's discomfort2 weeks

Countries

Italy

Outcome results

None listed

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