Viewing Study NCT02904551



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Study NCT ID: NCT02904551
Status: COMPLETED
Last Update Posted: 2019-08-16
First Post: 2016-09-09

Brief Title: Gingival Augmentation Around Implants During Maintenance
Sponsor: University of Maryland Baltimore
Organization: University of Maryland Baltimore

Study Overview

Official Title: Free Gingival Grafts for Implants Exhibiting Lack of Keratinized Gingiva A Prospective Controlled Randomized Clinical Study
Status: COMPLETED
Status Verified Date: 2019-08
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: This prospective controlled randomized blind clinical study investigated 44 implants displaying lack of KG in 29 subjects Fourteen subjects received FGGs followed by oral prophylaxis Fifteen subjects in the control group did not receive FGGs The width of KG gingival recession GR pocket depths PD plaque index PI and gingival index GI were assessed at baseline 6 12 and 18 months Changes in crestal bone levels from baseline were assessed at 18 months
Detailed Description: The purpose of this study was to evaluate clinical and radiographic outcomes following free gingival grafts FGGs around implants with limited keratinized gingiva KG compared to oral prophylaxis without gingival augmentation

This prospective controlled randomized blind clinical study investigated 44 implants displaying lack of KG in 29 subjects Fourteen subjects received FGGs followed by oral prophylaxis Fifteen subjects in the control group did not receive FGGs The width of KG gingival recession GR pocket depths PD plaque index PI and gingival index GI were assessed at baseline 6 12 and 18 months

There was a significant gain in KG with a reduction in GR in the FGG group compared to controls at 6 12 and 18 months The mean PI and GI were significantly lower for the FGG group at 12 and 18 months

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