Evaluation of a Lateral Window Technique Augmentation for Maxillary Sinus Using Ultrasound Activated Pins

Riyadh Colleges of Dentistry and Pharmacy

Status and phase: Unknown; Phase 4

Conditions: Tooth Loss

Treatments: Device: Resorb X Membrane; Procedure: Lateral Window Technique Augmentation for Maxillary Sinus; Device: Ultrasound activated resorbable poly-D-L-lactide pins; Device: Purus® Cancellous Allograft; Device: Biomend; Procedure: Trephine Biopsy; Procedure: Cone Beam CT image of the Sinus

Study type: Interventional

Funder types: Other

Identifiers

NCT02449707

FRP/2014/109

Details and patient eligibility

About

Ultrasound activated pins have been used for the promotion of bone healing in combination with biodegradable membranes during bone grafting procedures. In the jaws, these pins have been successfully tested for both maxillary and mandibular ridge augmentaton. However, the usefulness of these pins in maxillary sinus lift procedures has not been tested. This study aims to use a bilateral split mouth design to compare the bone formation, healing and post-operative complications after the use of ultrasonic guided pins in a lateral window maxillary sinus augmentation procedure in comparison to lateral window maxillary sinus augmentation procedure procedure performed without the use of these pins.

Full description

The study proposes to use a prospective split mouth crossover randomized control trial design to study the success of implant placement in cases with sinus lift procedures performed using the Sonic Weld® (KLS-Martin GmbH , Mulheim, Germany) ultrasound guided bone welding system with a membrane (Resorb X Membrane) on one side, and placement of Biomend collagen membrane to stabilize the graft

Patient selection:

20 patients requiring bilateral maxillary sinus lift procedure (40 procedures) will be selected from the patients reporting for implant placement to both the Riyadh Colleges of Dentistry and Pharmacy and the Riyadh Dental Center, King Saud Medical City.

Graft Placement:

Each patient will receive both the pin stabilized and the conventional graft placement procedures with standardized allografts (Purus® Cancellous Allograft?) on both sides of the maxilla. The grafts will be placed using the lateral window technique. The patients will be randomly assigned into either those who receive the pin first (Group A) or those who receive the conventional technique (using collagen membranes) first (Group B). The patients will have a one week gap between the sinus lift on the right and left sides.

Evaluations of the sinus lift procedure:

The sinus lift will be evaluated clinically radiographically and histologically using previously established criteria. Cone Beam CTs (Gallelios Comfort plus, Sirona Dental, Salzburg, Austria) will be taken preoperatively and at three month intervals to help assess the osseous outcomes of the graft.

At the end of one year the site will be evaluated clinically for the placement of implants. At the time of placement of the implant a trephine biopsy will be performed and H&E staining will be used to determine the histological outcomes of the graft procedure.

Statistical Analysis:

The paired t test will be used to compare the thickness of bone before and after the completion of the sinus lift procedure. The multiple measures paired ANOVA will be used to compare the thickness of bone at each follow up vist.

The student's t test will be used to compare the thickness of bone between the two types of sinus lift procedure.

The chi-square test will be used to compare differences (if any) in the histological patterns obtained at the end of the study.

Enrollment: 20 estimated patients

Sex: All

Ages: 45 to 55 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Loss of upper permanent molar on both right and left side
• Require Bilateral Maxillary Sinus Augmentation
• Consent to partipate in the study

Exclusion criteria

• History of Diabetes Mellitus (including patients who are controlled with oral hypoglyceamic drugs)
• Uncontrolled Hypertensive patients with three consecutive diastolic readings of over 90mmHg
• History of Osteoporosis

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Double Blind

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20 participants in 2 patient groups

Control

Active Comparator group

Description:

Lateral Window Technique Augmentation for Maxillary Sinus without the use of Ultrasound activated resorbable poly-D-L-lactide pins for the stabilization of membrane. Placement of Purus® Cancellous Allograft, stabilized by Biomend ™ Collagen membrane. Cone Beam CT image of the sinus will be taken to evaluate the bone formation. Trephine Biopsy will be performed after 1 year, at the time of placement of implant to check the quality of bone formed.

Treatment:

Procedure: Lateral Window Technique Augmentation for Maxillary Sinus

Procedure: Cone Beam CT image of the Sinus

Device: Purus® Cancellous Allograft

Procedure: Trephine Biopsy

Device: Biomend

Ultrasonic Pins

Experimental group

Description:

Lateral Window Technique Augmentation for Maxillary Sinus with the use of Ultrasound activated resorbable poly-D-L-lactide pins for the stabilization of the Purus® Cancellous Allograft, and Resorb X Membrane.Cone Beam CT image of the sinus will be taken to evaluate the bone formation. Trephine Biopsy will be performed after 1 year, at the time of placement of implant to check the quality of bone formed.

Treatment:

Procedure: Lateral Window Technique Augmentation for Maxillary Sinus

Procedure: Cone Beam CT image of the Sinus

Device: Purus® Cancellous Allograft

Procedure: Trephine Biopsy

Device: Ultrasound activated resorbable poly-D-L-lactide pins

Device: Resorb X Membrane