Actively Recruiting
Effect of Cyanoacrylate Tissue Adhesive Versus Collagen Sponge on Palatal Donor Site Healing
Led by Beirut Arab University · Updated on 2025-08-17
22
Participants Needed
1
Research Sites
37 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if the use of cyanoacrylate glue (PeriAcryl) is effective in healing of the palatal donor site in adults requiring a free gingival graft. The main question\[s\] it aims to answer \[is/are\]: Does PeriAcryl accelerate the palatal tissue healing compared with the use of collagen sponge? Does PeriAcryl usage leave the patients more satisfied? Researcher will compare the outcomes of participants treated with PeriAcryl to those treated with collagen sponge to see if PeriAcryl accelerated the healing process of palatal tissues and led to fewer postoperative complications. Participants will: * be assigned to a study group using PeriAcryl or control group using Collagen sponge. * be followed-up to monitor healing and gather clinical information.
CONDITIONS
Official Title
Effect of Cyanoacrylate Tissue Adhesive Versus Collagen Sponge on Palatal Donor Site Healing
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Low to moderate anesthetic risk (ASA I-II)
- No restriction on ethnicity or gender
- Patients needing a free gingival graft from the palate for periodontal plastic surgery
- Clinically healthy gums after initial therapy
- Full-mouth plaque index scores of 0 or 1
- Bleeding scores less than 15%
You will not qualify if you...
- Smoking more than 10 cigarettes per day
- Any bleeding or clotting disorders
- Presence of systemic diseases
- Use of medications that affect gum tissues
- Pregnancy or breastfeeding
- Allergies to prescribed medications during treatment
- Mental health conditions affecting cooperation (e.g., dementia, psychosis)
- Excessive gag reflex
AI-Screening
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Trial Site Locations
Total: 1 location
1
Beirut Arab University
Beirut, Lebanon
Actively Recruiting
Research Team
D
Dania EL Rostom, MSc Oral and Dental Surgery
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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