Clinical Investigation to Assess the Safety and Feasibility of the Crestal, Minimal-invasive Sinus Floor Augmentation With the Pressure Chamber Drill (DKK) and the Sinus Vibration Pump (SVP)
NCT01204424 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2010-09-17
Summary
The success of dental implants is based on a variety of factors including; surgical technique, health of the patient, operator skill and, to a significant part, sufficient bone for the placement and integration of dental implants. To that end, the replacement of the maxillary posterior teeth have presented a considerable challenge because, after the loss of maxillary posterior teeth the quality and quantity of the remaining supporting bone may be insufficient to support implants properly or reliably. To overcome the deficiency of insufficient vertical bone mass of the maxilla, several surgical techniques have been developed to increase available bone mass for the replacement of dental implants by bone augmentation.
The conventional procedure for a sinus lift (Caldwell-Luc procedure) requires preparation of a mucoperiosteal flap in the buccal molar region and to cut an oval window in the thus exposed bone, without damage to the subjacent maxillary sinus membrane. The procedure is very invasive and subjects the patient to great stress as a result of substantial swelling and discoloration of up to 10 days, and possibly of pain. This surgical procedure is oftentimes referred to as "open" or "classic" sinus lift. This technique is fraught with many risks and complications because of the limitations of healing potential in the maxillary sinus. In spite of these risks many patients undergo this procedure because of the strong desire to replace missing maxillary teeth with dental implants.
An alternative approach to the maxillary sinus from the inferior approach of the alveolar ridge utilizing solid cylindrical osteotomes was described by Dr. Summers (crestal sinus lift). It is a more conservative approach and is less invasive. It was developed to eliminate the risks described above.While this technique is safer, an overzealous use of an osteotome during the placement of the regenerative material can result in the perforation of the subantral membrane with disadvantages discussed above.
Dr. Eder has developed an innovative way - the JEDER System - of carrying out a crestal sinus lift that substantially reduces the risk of perforating the subantral membrane. This minimal- invasive way uses 2 newly developed and successfully patented instruments, the "Druckkammerknochenfräse" DKK and the "Sinusvibrationspumpe" SVP. Following JEDER Syst. the mucous membrane of the mouth is opened from the toothless part of the maxillary crest up to the bone and the bone is scraped by a cylindrical cutter in the shape of a tunnel up to slightly underneath the maxillary sinus membrane.
The aim of the study is to assess the efficacy and safety of the JEDER Syst., which was already demonstrated in 50 treatment attempts. The results of this study will be used for the certification process to enable the declaration of conformity for the market approval.
The main outcome parameter is the perforation rate of the subantral membrane intraoperatively and within 6 weeks after the operation.
Risk benefit assessment:
In the present study there will be no additional examinations undertaken compared to patients which undergo the conventional procedure. The conventional procedure is associated with a risk of membrane perforation and consecutive diseases like infection, swelling and pain. All these inconveniences should be avoided by using the JEDER Syst. If the worst case scenario - the perforation of the subantral membrane - happens, the conventional method will be used. Therefore, the risk-benefit assessment
Conditions
- Insufficient Bone Mass in the Maxilla for Dental Implants
Interventions
- DEVICE
-
minimal-invasive sinus floor augmentation with the DKK and SVP (JEDER Syst.)
minimal-invasive sinus floor augmentation with the DKK and SVP (JEDER Syst.)
- DEVICE
-
minimal invasive crestal sinus lift with the JEDER Systh.
The mucous membrane is opened from the toothless part of the maxillary crest up to the bone and the bone is scraped by a cylindrical cutter in the shape of a tunnel up to slightly underneath the maxillary sinus membrane and hydraulic pressure is being built up within the DKK. A centrally placed drill within the DKK slowly moves in the direction of the membrane. At the moment of the first minimal perforation of the remaining bone the pressurized fluid pushes the membrane back and ensures that the membrane is not perforated by the drill. The SVP is used to generate hydraulic vibrations, which help to further raise the membrane from the bone (principle of the "percussion drill"). After the maxillary sinus membrane has successfully been elevated, the working fluid is extracted and bone replacement material is introduced via the bore.
Sponsors & Collaborators
-
Jeder GmbH
lead INDUSTRY
Principal Investigators
-
Michaela M Bayerle-Eder, Prof., MD, MBA · Medical University Vienna, Vienna Austria, Europe
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-09-30
- Primary Completion
- 2011-03-31
- Completion
- 2011-06-30
Countries
- Austria
Study Locations
More Related Trials
-
Sinus Floor Elevation Using Separately Two Different Xenografts - A Prospective Randomized Clinical Trial
NCT01781221 ·Status: UNKNOWN ·Phase: NA
-
A Modified Sinus Floor Elevation Technique - a Pilot Study on 12 Patients
NCT02137824 ·Status: RECRUITING ·Phase: NA
-
Single Crown Supported by Short Implant Versus Standard Implant in Conjunction With Maxillary Sinus Floor Augmentation.
NCT04518020 ·Status: UNKNOWN ·Phase: NA
-
Implant Placement With Corticocancellous Bone Block vs Mineralized Plasmatic Matrix in Maxillary Sinus Lifting
NCT06073912 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Radiographic and Histomorphometric Assessment for Maxillary Sinus Floor Elevation and Augmentation Using A Mixture of 1:1 Autogenous Bone With Deproteinized Bovine Bone Particulate Versus Deproteinized Bovine Bone Particulate
NCT07177495 ·Status: RECRUITING ·Phase: NA
-
SINUS LIFT 100% Anorganic Bovine Bone vs. 50% Anorganic Bovine Bone + 50% Autologous Bone
NCT02170129 ·Status: COMPLETED ·Phase: NA
-
Hard and Soft Tissue Maintenance Around Implants With a Sloped Configuration
NCT04712565 ·Status: COMPLETED ·Phase: NA
-
Comparison of Straumann BoneCeramic vs. Allograft Bone in Extraction Sockets
NCT00782236 ·Status: TERMINATED ·Phase: PHASE4
-
Osteotome-mediated Sinus Floor Elevation With or Without Grafting Material
NCT04618900 ·Status: COMPLETED ·Phase: NA
-
Guided Bone Regeneration With Customized Titanium Meshes
NCT04480073 ·Status: UNKNOWN ·Phase: NA
-
Autogenous Mesenchymal Stem Cell Culture-Derived Signalling Molecules as Enhancers of Bone Formation in Bone Grafting
NCT04998058 ·Status: NOT_YET_RECRUITING ·Phase: PHASE1/PHASE2
-
3D Printed Models for Mandibular Fracture Repair
NCT05733221 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
A Comparative Study to Evaluate Bone Height Gain Following Transcrestal Sinus Floor Elevation Using Specially Designed Drills Versus the Conventional Osteotome Technique.
NCT02926781 ·Status: UNKNOWN ·Phase: NA
-
Advanced Intelligence Driven Drill for Maxillary Sinus Augmentation in Patients with Severe Bone Loss
NCT06731569 ·Status: COMPLETED ·Phase: NA
-
Effect of Multiple Perforations of the Sinus Floor on Bone Formation After Sinus Floor Elevation
NCT05362136 ·Status: RECRUITING ·Phase: NA
-
Effectiveness and Safety of Method of Maxilla Alveolar Process Reconstruction Using Synthetic Tricalcium Phosphate and Autologous MMSCs
NCT02209311 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Sinus Floor Augmentation and Graft Compared Sinus Membrane Elevation With Blood Coagulum. A Randomized Controlled Trial
NCT04667260 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
The Application of a Biphasic Calcium Sulfate Graft Material in Sinus Floor Elevation
NCT06533397 ·Status: RECRUITING ·Phase: NA
-
Pilot Study on Safety and Efficacy of MD05 in Comparison With Beta-TCP in Patients Undergoing Sinus Floor Augmentation
NCT00520377 ·Status: UNKNOWN ·Phase: PHASE2
-
Safety and Efficacy Evaluation of the Ivory Dentin Graft Device
NCT03150472 ·Status: COMPLETED ·Phase: NA
-
Mix of Demineralized Freeze-Dried Bone Allograft and Deproteinized Bovine Bone Mineral: a Possible Solution for Alveolar Ridge Preservation?
NCT06275789 ·Status: RECRUITING ·Phase: NA
-
Minimally Invasive Lateral Approach for Sinus Augmentation: a Split-mouth Randomized Clinical Trial.
NCT02117882 ·Status: COMPLETED
-
Maxillary Sinus Grafting With Deproteinized Porcine or Bovine Bone Mineral.
NCT05804253 ·Status: COMPLETED ·Phase: NA
-
Reliability of All on 4 Using 2 Zygomatic and 2 Conventional Implants vs All on 4 Implants for Rehabilitation of Maxilla
NCT05108324 ·Status: UNKNOWN ·Phase: NA
-
Performance and Safety of Bone Substitute MBCP-FS in Maxillary Sinus Lift Procedures
NCT00163605 ·Status: COMPLETED ·Phase: PHASE2/PHASE3