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

Tooth Loss Clinical Trial

Official title:

Evaluation of a Lateral Window Technique Augmentation for Maxillary Sinus Lift Using Ultrasound Activated Resorbable Poly-D-L-lactide Pins in Maxillary Sinus Lift - a Split Mouth Randomized Control Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02449707
• Other study ID #: FRP/2014/109
• Status: Recruiting
• Phase: Phase 4
• First received: May 14, 2015
• Last updated: May 16, 2015
• Start date: April 2015
• Est. completion date: August 2016

Study information

• Verified date: May 2015
• Source: Riyadh Colleges of Dentistry and Pharmacy
• Contact: Sharat Pani, MDS
• Phone: +966544981300
• Email: sharat[@]riyadh.edu.sa
• Is FDA regulated: No
• Health authority: Saudi Arabia: Ministry for Higher Education
• Study type: Interventional

Clinical Trial Summary

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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Est. completion date: August 2016
• Est. primary completion date: May 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 45 Years to 55 Years

Eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Tooth Loss

Intervention

Procedure:
• Lateral Window Technique Augmentation for Maxillary Sinus
Maxillary sinus augmentation will be performed using the lateral window technique

Device:
• Ultrasound activated resorbable poly-D-L-lactide pins
The titanium membrane placed during the maxillary sinus augmentation procedure will be stabilized using ultrasound activated resorbable poly-D-L-lactide pins
• Purus® Cancellous Allograft
Allograft material placed in the sinus to acheive sinus augmentation
• Resorb X Membrane
The membrane placed over the graft material before placement of the ultrasound activated pins
• Biomend
Collagen healing membrane placed over the graft material on the side where no ultrasound activated pins are being used

Procedure:
• Cone Beam CT image of the Sinus
Cone beam CT will used to assess the thickness of bone formation after the placement of the graft
• Trephine Biopsy
Trephine Biopsy will be performed at the time of the placement of implant to study the quality of bone formed

Locations

Country	Name	City	State
Saudi Arabia	Riyadh Colleges of Dentistry and Pharmacy	Riyadh

Sponsors (2)

Lead Sponsor	Collaborator
Riyadh Colleges of Dentistry and Pharmacy	King Saud Medical City

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in bone thickness (in mm)		Change from Baseline thickness in 6 months	No
Secondary	Change in Post-operative pain - as reported on a Visual Analog Scale (VAS)		Change from baseline VAS in 6 months	No
Secondary	Bone Quality - Measured by the type of bone observed on the trephine biopsy		1 year	No