Ignite Creation Date:
2025-12-24 @ 10:13 PM
Ignite Modification Date:
2025-12-25 @ 7:48 PM
Study NCT ID:
NCT04224935
Status:
COMPLETED
Last Update Posted:
2020-11-05
First Post:
2020-01-01
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
The Effect of (L-PRF) Membrane in The Treatment of Gingival Recession
Sponsor:
Ain Shams University
Organization:
Study Overview
Official Title:
The Effect of Leukocyte Platelet Rich Fibrin(L-PRF) Membrane in The Treatment of Localized Gingival Recession (Randomized Controlled Clinical Trial)
Status:
COMPLETED
Status Verified Date:
2020-11
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:
evaluation of the use of L-PRF membrane with coronally repositioned flap in treatment of localized gingival recession (Class I \& II) in comparison with the use of connective tissue graft
Detailed Description:
Twenty patients, who are candidates for gingival recession coverage, will participate in this prospective clinical trial.
Group 1(10 patients) :
Coronally repositioned flap will be done and L PRF membrane will be placed into the tissues
Group 2 (Control group)(10 patients) :
Coronally repositioned flap will be done with sub epithelial connective tissue Parameters
* Clinical evaluation of percentage of root coverage and keratinized tissue width
* Esthetic outcome evaluation Will be done using the root coverage esthetic score (Cairo et al. 2009) that include
Both evaluations will be done at 3, 6 and 9 months
Group 1(10 patients) :
Coronally repositioned flap will be done and L PRF membrane will be placed into the tissues
Group 2 (Control group)(10 patients) :
Coronally repositioned flap will be done with sub epithelial connective tissue Parameters
* Clinical evaluation of percentage of root coverage and keratinized tissue width
* Esthetic outcome evaluation Will be done using the root coverage esthetic score (Cairo et al. 2009) that include
Both evaluations will be done at 3, 6 and 9 months
Study Oversight
Has Oversight DMC:
True
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?: