About this trial
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.
Eligibility criteria
Qualifiers
Low-moderate anesthetic risk (ASA I-II)
No restriction on ethnicity or gender
Patients requiring FGG from the palate for periodontal plastic surgery
Clinically healthy gingiva after phase I therapy
Disqualifiers
Patients who smoke > 10 cigarettes/day
Patients with coagulation disorders
Systemic diseases
Patients on certain medications that may affect periodontal tissues
Trial design
Treatments tested in this trial
- Cyanoacrylate tissue adhesive
- Collagen sponge