Ignite Creation Date:
2024-05-06 @ 8:13 PM
Last Modification Date:
2024-10-26 @ 3:23 PM
Study NCT ID:
NCT06297577
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-03-18
First Post:
2024-02-18
Brief Title:
Clinical Evaluation of Injectable Alb-PRF in the Management of Intrabony Defect in Stage-III Periodontitis Patients
Sponsor:
Cairo University
Organization:
Cairo University
Study Overview
Official Title:
Clinical Evaluation of Injectable Albumin Platelet Rich Fibrin Alb-PRF Versus Minimally Invasive Surgical Technique MIST in the Management of Intra-bony Defect in Stage-III Periodontitis Patients A Randomized Controlled Clinical Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
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:
Clinical Evaluation of Injectable Albumin Platelet Rich Fibrin Versus Platelet Rich Fibrin in the Management of Intra-bony Defect in Stage-III Periodontitis Patients
The goal of this clinical trial is to compare Injectable Albumin Platelet Rich Fibrin Versus Platelet Rich Fibrin in the Management of Intra-bony Defect in Stage-III Periodontitis Patients The main question aims to answer are
will Albumin Platelet Rich Fibrin Alb-PRF as adjunct to minimally invasive surgical technique MIST be superior in terms of improvement in clinical parameters compared to the use of PRF with MIST
The goal of this clinical trial is to compare Injectable Albumin Platelet Rich Fibrin Versus Platelet Rich Fibrin in the Management of Intra-bony Defect in Stage-III Periodontitis Patients The main question aims to answer are
will Albumin Platelet Rich Fibrin Alb-PRF as adjunct to minimally invasive surgical technique MIST be superior in terms of improvement in clinical parameters compared to the use of PRF with MIST
Detailed Description:
None
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