Ignite Creation Date:
2024-10-25 @ 7:58 PM
Last Modification Date:
2024-10-26 @ 3:40 PM
Study NCT ID:
NCT06593275
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-09
Brief Title:
Pain Perception in Protection of the Palatal Donor Area After Harvesting a Free Gingival Graft Using Flowable Resin Versus a Self-adhesive Dressing
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Pain Perception in Protection of the Palatal Donor Area After Harvesting a Free Gingival Graft Using Flowable Resin Versus a Self-adhesive Dressing
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:
The use of a connective tissue graft harvested from the palate is currently one of the most effective and predictable alternatives for the correction of periodontal and peri-implant defects but the discomfort generated in the palate is sometimes greater than mucogingival surgery For this reason we found the need to use different materials for palatal protection In one group we will use light-cured fluid resin compared to another group a self-adhesive dressing to check which of these materials provides less postoperative pain generated by the harvest of a free gingival graft
Detailed Description:
The postoperative pain generated by the harvest of a free gingival graft for the correction of periodontal or peri-implant defects it39s greater when it is not adequately protected and until the reepithelialization of the area is complete For this reason it was decided to use two materials to compare the effectiveness in reducing postoperative pain in grafts larger than 15 mm A control group will be treated with a hemostatic collagen sponge and photocured fluid resin adhered to the palatal surfaces of the neighboring teeth using an adhesive protocol and X-shaped sutures Another experimental group will be treated with a hemostatic sponge and placement of a self-adhesive dressing stabilized by X-shaped sutures to ensure its permanence in the mouth The participants will fill out a daily visual analog scale form for 14 days until the removal of the materials Finally the results will be tabulated and compared to provide a conclusion of our study
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