Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06522321
Status:
ENROLLING_BY_INVITATION
Last Update Posted:
None
First Post:
2024-07-22
Brief Title:
Radiographic Assessment of Bone Dimension Around Immediate Implants With FDBA and I-PRF vs FDBA Alone
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Radiographic Assessment of Bone Dimension Around Immediate Implants With FDBA and I-PRF vs FDBA Alone- A Randomized Clinical Controlled Trial
Status:
ENROLLING_BY_INVITATION
Status Verified Date:
2024-07
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:
The present study is a human prospective parallel randomised controlled clinical trial conducted for radiographic assessment of bone dimension around immediate implants with FDBA and I-PRF vs FDBA Alone The trial is in accordance with the Consolidated Standards of Reporting Trials CONSORT criteria 2010
Detailed Description:
Twenty healthy individuals satisfying the inclusion and exclusion criteria were recruited for the study A detailed thorough medical and dental history was obtained and each patient was subjected to comprehensive clinical and radiological examination All patients were informed about the nature of the study the surgical procedure involved potential benefits and risks associated with the surgical procedure and written informed consent were obtained from all patients All the patients were treated with immediate implants in endodontically and periodontically compromised sites FDBA graft along with I-PRF is combined to form a sticky bone this stable element is placed around the implants where bone is compromised
The clinical and radiographic parameters were recorded at baseline three months and six months postoperatively
The clinical and radiographic parameters were recorded at baseline three months and six months postoperatively
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