Clinical Trials Directory

Trials / Completed

CompletedNCT06806566

Assessment of a Carvacrol-loaded Absorbable Gelatin Sponge Used as a Palatal Dressing Following Free Gingival Graft Harvesting.

Clinical Evaluation of Carvacrol Loaded Absorbable Gelatin Sponge as a Palatal Bandage After Free Gingival Graft Harvesting .

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
British University In Egypt · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

To evaluate the effect of carvacrol loaded to absorbable gelatin sponge as a palatal bandage on the palatal donor site in post-operative pain reduction after free gingival graft harvesting

Conditions

Interventions

TypeNameDescription
OTHERCarvacrol1-absorbable gelatine sponge soaked in carvacrol oil placed in the palatal donor site. Procedure: The palatal sites will be anaesthetized with 0.3 ml of a solution of 4% Articaine and 0.001% Adrenalin. Graft harvesting will be performed by basic surgical techniques previously described by Miller (1982). A rectangular shaped piece of mucosa will be harvested from the area of the hard palate by a split-thickness dissection. The graft will then be used as it on the recipient bed. The graft dimensions will be recorded (width and length). Denuded palatal area will then be protected using a carvacrol loaded absorbable gelatin sponge (test group)
OTHERGelatin Sponge SheetAbsorbable gelatin sponge placed in the palatal donor site Procedure: The palatal sites will be anaesthetized with 0.3 ml of a solution of 4% Articaine and 0.001% Adrenalin. Graft harvesting will be performed by basic surgical techniques previously described by Miller (1982). A rectangular shaped piece of mucosa will be harvested from the area of the hard palate by a split-thickness dissection. The graft will then be used as it on the recipient bed. The graft dimensions will be recorded (width and length). Denuded palatal area will then be protected using a absorbable gelatin sponge(control group).

Timeline

Start date
2024-02-01
Primary completion
2025-05-01
Completion
2025-05-01
First posted
2025-02-04
Last updated
2026-04-06

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06806566. Inclusion in this directory is not an endorsement.