Ignite Creation Date:
2024-05-06 @ 11:58 AM
Last Modification Date:
2024-10-26 @ 12:52 PM
Study NCT ID:
NCT03640910
Status:
COMPLETED
Last Update Posted:
2021-02-09
First Post:
2018-03-29
Brief Title:
Attachment Systems for Implant Overdenture
Sponsor:
Rhein 83 Srl
Organization:
Rhein 83 Srl
Study Overview
Official Title:
A Cluster-randomized Multicenter Trial Comparing OT-Equator Versus Locator Attachments to Retain an Early Loaded Implant Overdenture on Two or Three Implants
Status:
COMPLETED
Status Verified Date:
2021-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The aim of this randomized controlled trial is to compare peri-implant tissue health number of complications and patients preference between two unsplinted overdenture attachments
Detailed Description:
Study design A cluster-randomized multicenter trial of parallel group design and two arms Patients with complete edentulous mandible in needed of an implant retained overdenture will be randomly clustered to receive two or three unsplinted implants Afterwards patients that have been randomized to receive two implants will be randomized to receive OT Equator attachment Rhein83 Bologna Italy in the test group or Locator attachment Zest Anchors LLC Espandido CA USA in the control group
Patients will be selected and consecutively treated in 10 private and public University centers in Europe between December 2017 and December 2018 This study will be conducted in accordance with the principles outlined in the Helsinki Declaration of 1964 for biomedical research involving human subjects as amended in 2013 and will receive ethical approval by Ethical Committees of the various centers Patients will be duly informed about the nature of the study A written informed consent form for surgical and prosthetic procedures as well as for the use of the clinical and radiological data will be obtained for each patient The present research will be registered in the Clinical trialgov and the manuscript will be written according to the CONSORT guidelines
Any healthy individual ASA 1 and 2 aged 18 years or older at the time of enrollment with complete edentulous mandible or a failing dentition in the mandible scheduled to receive an implant supported overdenture will be considered eligible for the study Exclusion criteria are the general contraindications to oral surgery pregnancy or nursing intravenous bisphosphonate therapy alcohol or drug abuse heavy smoking 20 cigarettesday radiation therapy to the head or neck region within the last five years parafunctional activity untreated periodontitis and allergy or adverse reactions to the restorative materials
Preoperative photographs panoramic x-rays and periodontal screening have to be obtained for initial screening and evaluation Hopeless teeth in the mandible have to be extracted 3 months before implant placement and new prosthesis delivery All of the patients will receive a temporary complete removable denture before implant placement according to the respective functional and esthetic requirements If the actual complete removable denture is judged accurate from both patients and clinician it could be used as temporary solution
On the day of the surgery a single dose of an antibiotic either 2 g of amoxicillin or 600 mg of clindamycin or 500 mg of azitromicin or claritromicin if allergic to penicillin will be administered 1 h before implant placement 2017 AHA Immediately before surgery the participants will rinse with a 02 chlorhexidine mouthwash for 1 min Local anesthesia preferred by the surgeon will be administered Flapless or a minimally invasive mucoperiosteal flaps will be elevated Then the patients will be randomly clustered to receive two or three unsplinted implants according to congealed indication contained in a close enveloped and derived from a pre-generated list Afterwards only the patients that will be randomized to receive two implants will be randomized to receive OT Equator attachment Rhein83 Bologna Italy in the test group or Locator attachment Zest Anchors LLC Espandido CA USA in the control group
Implants have to be placed in the interforaminal region of the mandible according to a one-stage approach
Three-IRO center implant will be placed in the midline and the distal implants were placed 11 mm distal aligned at a 0-20-degree inclination corresponding to the center implants with up to an extensive 40 degrees of divergence between implants them
Two-IRO implants will be placed in the canine region of the mandible with an interconnecting line approaching parallelism with the terminal mandibular hinge axis and an extensive 40 degrees of divergence between implants them
Any brand of implants that provide either Locator or OT-Equator abutments can be placed according to the manufacturer suggestions in order to achieve an insertion torque of at least 35 N cm The implant lengths will be dictated by the preoperative radiographs Jaw bone quality will be rated during the dental implant surgery by the tactile resistance during drilling allowing an objective evaluation according to the Lekholm Zarb index
After surgery the patients will be instructed to avoid brushing and trauma at the surgical site A post-surgical cold and soft diet will be recommended Smokers will be recommended to avoid smoking for 2 weeks days postoperatively and oral hygiene instructions will be given Chlorhexidine 012 rinses 3 timesday Analgesics 600 mg of ibuprofen or other will be prescribed as needed Sutures if present will be removed after ten days
The prosthetic procedures will begin eight weeks after implant placement A reliable fully extended impressions of both jaws will be taken Then a definitive polysulfide-based or polyether impression will be made by using a customized acrylic resin tray and master cast will be poured with low expansion class IV gypsum Intermaxillary relation using registration plates or clinical bite index functional occlusal analysis face-bow and occlusal vertical dimension have to be taken Master cast and antagonists will be mounted in a semi adjustable articulator and a diagnostic prosthetic setup will be made and tried in the patients mouth in which the functional and aesthetic parameters will be evaluated
A new metal reinforced complete removable denture will be delivered in both groups within 4 weeks after second surgery according to an early loading protocol The healing abutments will be unscrewed and the implant connections have to be disinfected Randomized attachment system will be placed and tightened according to the manufacturer
Test Group OT Equator
After gingival healing the newest low-profile OT Equators Rhein83 will be screwed on to the implants using the OT Equator square screwdriver Rhein83 with a torque range of 22-25 N cm The cuff heights ranged from 05 to 70 mm depending on the height of the transition zone of each implant easily measured using the color-coded millimeter Cuff Height Measurer Gauge Rhein83 after healing abutment removal Afterward spaces to accept the female housing steel cage will be prepared in the fitting surface of the removable complete mandibular denture Silicone protective discs Rhein83 will be placed over the OT Equator attachments Extra-soft yellow 600 g retentive caps will be initially placed in to the female steel housing attached to the OT Equator and finally fixed to the denture using self-cured acrylic resin while the patient held the dentures in occlusion directly chairside After complete polymerization the denture will be picked up and silicone discs removed Acrylic excess will be trimmed and the denture will be refined and polished One month after prosthesis delivery the yellow retentive caps will be replaced with a stronger type pink 1200 g
Control Group Locators The low-profile attachments Locator Zest will be screwed on to the implants using the Locator screwdriver Zest with a torque range of 20-25 N cm The cuff heights of 25 or 40 mm depending on the height of the transition zone of each implant measured using the deep probe of the implant line after healing abutment removal Afterward spaces to accept the female housing steel cage will be prepared in the fitting surface of the removable complete mandibular denture Silicone protective white rings Zest will be placed over the Locator attachments Passive black caps will be used to load the attachment Attached to the Locator and finally fixed to the denture using self-cured acrylic resin while the patient held the dentures in occlusion directly chairside After complete polymerization the denture will be picked up and white rings removed Acrylic excess will be trimmed and the denture will be refined and polished Black caps will be removed and blue ones 6N will be mounted in the steel housing One month after prosthesis delivery the retentive caps will be replaced with a pink matrix 12N
In both groups the occlusion will be developed to deliver a lingualized occlusion with balanced contacts during function avoiding any premature contacts Nevertheless when the opposing arch is a removable complete denture the over-jet has to be left purposely broad from 2 to 5 mm in order to avoid interferences during function Instructions will be given to the patients and recall visits will be scheduled for occlusal adjustments and oral hygiene quality control every six months and for retentive cap replacement every year
Outcomes implant and prosthetic success and survival rate biologic and technical complications marginal bone loss patients satisfaction Oral Health Impact Profile OHIP-22
Patients will be selected and consecutively treated in 10 private and public University centers in Europe between December 2017 and December 2018 This study will be conducted in accordance with the principles outlined in the Helsinki Declaration of 1964 for biomedical research involving human subjects as amended in 2013 and will receive ethical approval by Ethical Committees of the various centers Patients will be duly informed about the nature of the study A written informed consent form for surgical and prosthetic procedures as well as for the use of the clinical and radiological data will be obtained for each patient The present research will be registered in the Clinical trialgov and the manuscript will be written according to the CONSORT guidelines
Any healthy individual ASA 1 and 2 aged 18 years or older at the time of enrollment with complete edentulous mandible or a failing dentition in the mandible scheduled to receive an implant supported overdenture will be considered eligible for the study Exclusion criteria are the general contraindications to oral surgery pregnancy or nursing intravenous bisphosphonate therapy alcohol or drug abuse heavy smoking 20 cigarettesday radiation therapy to the head or neck region within the last five years parafunctional activity untreated periodontitis and allergy or adverse reactions to the restorative materials
Preoperative photographs panoramic x-rays and periodontal screening have to be obtained for initial screening and evaluation Hopeless teeth in the mandible have to be extracted 3 months before implant placement and new prosthesis delivery All of the patients will receive a temporary complete removable denture before implant placement according to the respective functional and esthetic requirements If the actual complete removable denture is judged accurate from both patients and clinician it could be used as temporary solution
On the day of the surgery a single dose of an antibiotic either 2 g of amoxicillin or 600 mg of clindamycin or 500 mg of azitromicin or claritromicin if allergic to penicillin will be administered 1 h before implant placement 2017 AHA Immediately before surgery the participants will rinse with a 02 chlorhexidine mouthwash for 1 min Local anesthesia preferred by the surgeon will be administered Flapless or a minimally invasive mucoperiosteal flaps will be elevated Then the patients will be randomly clustered to receive two or three unsplinted implants according to congealed indication contained in a close enveloped and derived from a pre-generated list Afterwards only the patients that will be randomized to receive two implants will be randomized to receive OT Equator attachment Rhein83 Bologna Italy in the test group or Locator attachment Zest Anchors LLC Espandido CA USA in the control group
Implants have to be placed in the interforaminal region of the mandible according to a one-stage approach
Three-IRO center implant will be placed in the midline and the distal implants were placed 11 mm distal aligned at a 0-20-degree inclination corresponding to the center implants with up to an extensive 40 degrees of divergence between implants them
Two-IRO implants will be placed in the canine region of the mandible with an interconnecting line approaching parallelism with the terminal mandibular hinge axis and an extensive 40 degrees of divergence between implants them
Any brand of implants that provide either Locator or OT-Equator abutments can be placed according to the manufacturer suggestions in order to achieve an insertion torque of at least 35 N cm The implant lengths will be dictated by the preoperative radiographs Jaw bone quality will be rated during the dental implant surgery by the tactile resistance during drilling allowing an objective evaluation according to the Lekholm Zarb index
After surgery the patients will be instructed to avoid brushing and trauma at the surgical site A post-surgical cold and soft diet will be recommended Smokers will be recommended to avoid smoking for 2 weeks days postoperatively and oral hygiene instructions will be given Chlorhexidine 012 rinses 3 timesday Analgesics 600 mg of ibuprofen or other will be prescribed as needed Sutures if present will be removed after ten days
The prosthetic procedures will begin eight weeks after implant placement A reliable fully extended impressions of both jaws will be taken Then a definitive polysulfide-based or polyether impression will be made by using a customized acrylic resin tray and master cast will be poured with low expansion class IV gypsum Intermaxillary relation using registration plates or clinical bite index functional occlusal analysis face-bow and occlusal vertical dimension have to be taken Master cast and antagonists will be mounted in a semi adjustable articulator and a diagnostic prosthetic setup will be made and tried in the patients mouth in which the functional and aesthetic parameters will be evaluated
A new metal reinforced complete removable denture will be delivered in both groups within 4 weeks after second surgery according to an early loading protocol The healing abutments will be unscrewed and the implant connections have to be disinfected Randomized attachment system will be placed and tightened according to the manufacturer
Test Group OT Equator
After gingival healing the newest low-profile OT Equators Rhein83 will be screwed on to the implants using the OT Equator square screwdriver Rhein83 with a torque range of 22-25 N cm The cuff heights ranged from 05 to 70 mm depending on the height of the transition zone of each implant easily measured using the color-coded millimeter Cuff Height Measurer Gauge Rhein83 after healing abutment removal Afterward spaces to accept the female housing steel cage will be prepared in the fitting surface of the removable complete mandibular denture Silicone protective discs Rhein83 will be placed over the OT Equator attachments Extra-soft yellow 600 g retentive caps will be initially placed in to the female steel housing attached to the OT Equator and finally fixed to the denture using self-cured acrylic resin while the patient held the dentures in occlusion directly chairside After complete polymerization the denture will be picked up and silicone discs removed Acrylic excess will be trimmed and the denture will be refined and polished One month after prosthesis delivery the yellow retentive caps will be replaced with a stronger type pink 1200 g
Control Group Locators The low-profile attachments Locator Zest will be screwed on to the implants using the Locator screwdriver Zest with a torque range of 20-25 N cm The cuff heights of 25 or 40 mm depending on the height of the transition zone of each implant measured using the deep probe of the implant line after healing abutment removal Afterward spaces to accept the female housing steel cage will be prepared in the fitting surface of the removable complete mandibular denture Silicone protective white rings Zest will be placed over the Locator attachments Passive black caps will be used to load the attachment Attached to the Locator and finally fixed to the denture using self-cured acrylic resin while the patient held the dentures in occlusion directly chairside After complete polymerization the denture will be picked up and white rings removed Acrylic excess will be trimmed and the denture will be refined and polished Black caps will be removed and blue ones 6N will be mounted in the steel housing One month after prosthesis delivery the retentive caps will be replaced with a pink matrix 12N
In both groups the occlusion will be developed to deliver a lingualized occlusion with balanced contacts during function avoiding any premature contacts Nevertheless when the opposing arch is a removable complete denture the over-jet has to be left purposely broad from 2 to 5 mm in order to avoid interferences during function Instructions will be given to the patients and recall visits will be scheduled for occlusal adjustments and oral hygiene quality control every six months and for retentive cap replacement every year
Outcomes implant and prosthetic success and survival rate biologic and technical complications marginal bone loss patients satisfaction Oral Health Impact Profile OHIP-22
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None