Ignite Creation Date:
2024-05-06 @ 8:02 AM
Last Modification Date:
2024-10-26 @ 11:55 AM
Study NCT ID:
NCT02656732
Status:
COMPLETED
Last Update Posted:
2017-04-24
First Post:
2016-01-13
Brief Title:
Amnion Chorion Membrane in Comparison to Subepithelial Connective Tissue Graft in Gingival Recession Coverage
Sponsor:
Cairo University
Organization:
Cairo University
Study Overview
Official Title:
Clinical Evaluation of Amnion Chorion Membrane in Comparison to Subepithelial Connective Tissue Graft in Gingival Recession Coverage A Randomized Controlled Clinical Trial
Status:
COMPLETED
Status Verified Date:
2017-04
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:
The present randomized controlled parallel-grouped trial included twenty patients aged 20 to 54 years suffering from Millers class I or II gingival recession Patients were randomly assigned into two equal groups control group the coronally advanced flap with the subepithelial connective tissue graft CAFSCTG or the test group coronally advanced flap with amnion chorion allograft membrane CAFAC
Detailed Description:
The participants were randomly assigned to receive coronally advanced flap CAF with amnion chorion membrane or CAF with subepithelial connective tissue graft using a simple randomization procedure with a 11 allocation ratio A computer generated randomization list was drawn up by a faculty member who was not involved in the recruitment Allocation concealment was achieved by sealed coded opaque envelopes that contained the treatment to be performed to the enrolled subjects based on the randomized numbers Consequently patients were allocated to either AC membrane intervention or SCTG control groups The sealed envelope containing treatment assignment was opened at time of the surgery and the number was picked by another person other than the operator
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