Ignite Creation Date:
2024-10-26 @ 3:43 PM
Last Modification Date:
2024-10-26 @ 3:43 PM
Study NCT ID:
NCT06646432
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-10-03
Brief Title:
Treatment of Gingival Recession With Tunnel Technique Using Connective Tissue Graft and Injectable Platelet Rich Fibrin
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Treatment of Gingival Recession by Tunnel Technique Using Connective Tissue Graft With or Without Injectable Platelet Rich Fibrin A Randomized Controlled Clinical Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
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:
Gingival recession is a common periodontal problem Consequences include teeth sensitivity poor esthetics and impaired oral hygiene access Mild cases are managed by optimizing oral hygiene measures correction of any causative factor such as faulty tooth brushing improper dental restoration or denture clasp Prescription of desensitization products such as specific tooth gels or mouth washes can manage the sensitivity problem Deeper recession defects need to be addressed by surgical procedures Coronally advanced flap with connective tissue graft is the gold standard procedure However it has some drawbacks due to the need for papillary incisions and vertical incisions in some cases Within the era of minimally invasive periodontology tunnel technique with connective tissue graft showed results comparable to coronally advanced flap with connective tissue graft but with some limitations Addition of another agent may enhance the results of tunnel technique Injectable platelet rich fibrin is known for its content of growth factors and effects on soft tissue healing Aim The study aim is to compare the surgical management of gingival recession with tunnel technique using connective tissue graft and injectable platelet rich fibrin to tunnel with connective graft without injectable platelet rich fibrin
Methodology 30 patients with miller class I or II gingival recession will be enrolled 15 in the test group Tunnel CTG i-PRF and 15 in control group Tunnel CTG Clinical evaluation at 6 months
Methodology 30 patients with miller class I or II gingival recession will be enrolled 15 in the test group Tunnel CTG i-PRF and 15 in control group Tunnel CTG Clinical evaluation at 6 months
Detailed Description:
30 patients with miller class III gingival recession will be enrolled in this study
15 patients will be treated using tunnel technique and palatal connective tissue graft inserted and sutured under the prepared tunnel after being soaked in injectable platelet rich fibrin for 15 minutes The tunnel with the underlying graft will be advanced coronally Test Group The other 15 patients will be treated the same way as in the first group but without soaking the graft in injectable platelet rich fibrin Control Group Clinical parameters will be evaluated at baseline and 6 months follow-up except post-operative pain which will be assessed after 10 days Histologic examination of small piece of the graft will be done to assess if there is true saturation of growth factors inside the graft
15 patients will be treated using tunnel technique and palatal connective tissue graft inserted and sutured under the prepared tunnel after being soaked in injectable platelet rich fibrin for 15 minutes The tunnel with the underlying graft will be advanced coronally Test Group The other 15 patients will be treated the same way as in the first group but without soaking the graft in injectable platelet rich fibrin Control Group Clinical parameters will be evaluated at baseline and 6 months follow-up except post-operative pain which will be assessed after 10 days Histologic examination of small piece of the graft will be done to assess if there is true saturation of growth factors inside the graft
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