Ignite Creation Date:
2024-05-06 @ 8:14 PM
Last Modification Date:
2024-10-26 @ 3:23 PM
Study NCT ID:
NCT06302387
Status:
COMPLETED
Last Update Posted:
2024-03-08
First Post:
2024-02-21
Brief Title:
Acellular Dermal Matrix Versus Tenting Technique in Peri-implant Soft Tissue Augmentation and Crestal Bone Stability
Sponsor:
Harvard Medical School HMS and HSDM
Organization:
Harvard Medical School HMS and HSDM
Study Overview
Official Title:
Efficacy of Acellular Dermal Matrix Versus Tenting Technique in Peri-implant Soft Tissue Augmentation and Crestal Bone Stability A Randomized Clinical Trial
Status:
COMPLETED
Status Verified Date:
2024-03
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:
This study looks at two ways to make gums thicker and bones stable around dental implants for people with thin gums It compares two methods in 40 people one method uses a special graft and the other uses a technique called tenting The goal is to see which method might work better for making the gums and bones around implants healthier The check-ups are planned when the implant is put in and again after one year The study focuses on how these methods are done without talking about what the results are
Detailed Description:
The studys protocol entails a randomized comparison between acellular dermal matrix grafting and the tenting technique aimed at enhancing gum thickness and bone stability around dental implants in individuals with thin gum profiles Forty participants are systematically assigned to one of the two methods under investigation The study is structured to evaluate the interventions potential in improving conditions conducive to the success of dental implants specifically targeting soft tissue thickness and crestal bone level stability The comprehensive investigation is designed to explore effective approaches for managing patients with particular soft tissue challenges focusing on the clinical application and procedural aspects without presenting any results or conclusions
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