Ignite Creation Date:
2024-06-16 @ 11:51 AM
Last Modification Date:
2024-10-26 @ 3:32 PM
Study NCT ID:
NCT06455436
Status:
RECRUITING
Last Update Posted:
2024-06-12
First Post:
2024-05-30
Brief Title:
Dimensional Changes of Peri-implant Tissue in Immediate Implants With Individualized Healing Abutments
Sponsor:
Universitat Internacional de Catalunya
Organization:
Universitat Internacional de Catalunya
Study Overview
Official Title:
Dimensional Changes of Peri-implant Tissue in Immediate Implants With Individualized Healing Abutments Using a CADCAM Technique Randomized Controlled Clinical Trial
Status:
RECRUITING
Status Verified Date:
2024-05
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 loss of a tooth leads to a series of biological changes in the tissues resulting in bone resorption and gingival collapse To avoid these problems it has been proposed to place immediate post-extraction implants allowing a reduction in treatment time and the number of surgeries as well as better maintenance of the tissues This technique can be performed with standard abutments after implant placement or more recently the use of temporary abutments has been proposed
Detailed Description:
Objective To check if custom healing abutments manufactured using CADCAM technique in immediate implants promote greater dimensional stability of the peri-implant tissue compared to standard healing abutments
Methods After the extraction an immediate Klockner Vega implant will be placed and the gap will be filled with a bone substitute Cerabone Botiss The patient will then be randomized to the control group standard healing abutment or the test group custom healing abutment using CADCAM technique In the latter case a peripheral seal is achieved allowing for wound closure and stabilization of the clot with the same shape as the crown in its transmucosal part
Methods After the extraction an immediate Klockner Vega implant will be placed and the gap will be filled with a bone substitute Cerabone Botiss The patient will then be randomized to the control group standard healing abutment or the test group custom healing abutment using CADCAM technique In the latter case a peripheral seal is achieved allowing for wound closure and stabilization of the clot with the same shape as the crown in its transmucosal part
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