Ignite Creation Date:
2024-10-26 @ 3:40 PM
Last Modification Date:
2024-10-26 @ 3:40 PM
Study NCT ID:
NCT06599112
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-08-16
Brief Title:
Clinical and Radiographic Evaluation of Implant Stability in Healed Maxillary Posterior Sites Comparing Osteotome Osseodensification and Conventional Drilling Implant Placement Techniques
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Clinical and Radiographic Evaluation of Implant Stability in Healed Maxillary Posterior Sites Comparing Osteotome Osseodensification and Conventional Drilling Implant Placement Techniques A Randomized Clinical Trial
Status:
RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study aims to compare the implant stability values following implant placement via Osteotomes and via Osseodensification using Densah Burs versus implant placement using conventional drilling technique in patients with upper posterior partially edentulous ridges as well as evaluating the crestal bone loss around temporary restorations following the three compared drilling techniques
Detailed Description:
Patients with partially edentulous ridges seeking restoration of their missing teeth with enough measurements for implant placement will be recruited from the outpatient clinic of the Oral Medicine and Periodontology Department Faculty of Dentistry-Cairo University to participate in this study and will be randomized to be either undergoing conventional drilling according to the manufacturers instructions control group or either one of the two intervention groups Intervention group A where implant placement will be done using the Osseodensification technique by the Densah burs or Intervention group B where the implant placement will be done using the Osteotomes
Neobiotech IS III active implants will be used in this study they have an osseoconductive SLA-coated surface a tapered design with a crestal macrothread design 08 pitch a self compactable apex as well as deep thread to maximize implant stability The implant has a platform switching feature and a conicalhex design
A temporary PMMA crown after 3 months from implant placement and will be kept for follow up for a year then definitive final restoration will be made
Neobiotech IS III active implants will be used in this study they have an osseoconductive SLA-coated surface a tapered design with a crestal macrothread design 08 pitch a self compactable apex as well as deep thread to maximize implant stability The implant has a platform switching feature and a conicalhex design
A temporary PMMA crown after 3 months from implant placement and will be kept for follow up for a year then definitive final restoration will be made
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None