Viewing Study NCT06530199



Ignite Creation Date: 2024-10-25 @ 7:55 PM
Last Modification Date: 2024-10-26 @ 3:36 PM
Study NCT ID: NCT06530199
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-07-19

Brief Title: Simplified Papilla Preservation FlapSPPF and Enamel Matrix DerivativeEMD With or Without Connective TissueCTG Wall for the Treatment of Non Contained Infrabony Defects A Randomized Controlled Clinical Trail
Sponsor: None
Organization: None

Study Overview

Official Title: Simplified Papilla Preservation FlapSPPF and Enamel Matrix DerivativeEMD With or Without Connective TissueCTG Wall for the Treatment of Non Contained Infrabony Defects A Randomized Controlled Clinical Trail
Status: NOT_YET_RECRUITING
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: Research is to compare and evaluate the clinical and radiographic outcomes of the enamel matrix derivative with or without connective tissue wall graft for noncontained infrabony defects using simplified papilla preservation technique
Detailed Description: Research is to compare and evaluate the clinical and radiographic outcomes of the enamel matrix derivative with or without connective tissue wall graft for noncontained infrabony defects using simplified papilla preservation technique The objectives is to assess the probing pocket depth reduction clinical attachment level gaingingival recession depth and radiographic bone gain The TEST group will be treated withSIMPLIFIED PAPILLA PRESERVATION flap with connective tissue graft and enamel matrix derivative and the CONTROL group will be treated with SIMPLIFIED APILLA PRESERVATION flap and enamel matrix derivative The total number of participants included will be 30 Control-15 Study-15 with a 6 month follow up

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