The Effect of Two Different Approaches on Palatal Donor Site
1 other identifier
interventional
50
1 country
1
Brief Summary
An epithelialized gingival graft will be harvested from the palate for the treatment of various mucogingival deformities. The donor site will be treated with either a combination of a collagen sponge, cyanoacrylate and suspending sutures or a collagen sponge, cyanoacrylate, suspending sutures and coconut oil.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 10, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 20, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
May 20, 2024
CompletedFirst Submitted
Initial submission to the registry
September 1, 2024
CompletedFirst Posted
Study publicly available on registry
September 3, 2024
CompletedSeptember 3, 2024
September 1, 2024
7 months
September 1, 2024
September 1, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Donor site pain perception
Patients score their daily donor site pain perception using visual analog score level by giving numbers from 0 to 10 according to the visual analog scale (0: no pain, 1: minimal pain, 10: severe pain)
everyday in first week
Secondary bleeding time
Patients will record presence or absence of secondary bleeding (presence=1 or absence=0).
during first week
Secondary Outcomes (9)
Graft height
during surgery
Graft width
during surgery
Graft thickness
during surgery
Working time
during surgery
Quantity of analgesics
first week
- +4 more secondary outcomes
Study Arms (2)
gelatin sponge + cyanoacrylate + suspending sutures
ACTIVE COMPARATORAfter administration of local anesthesia (2% articaine hydrochloride with epinephrine 1:100,000), palatal thickness will be measured by perpendicularly inserting a Michigan-O periodontal probe from the corners of the rectangular donor area. Epithelialized gingival graft will be harvested. After a rectangular-shaped initial incision, a graft with 1-1.5 mm thickness will be harvested approximately 1.5 to 3 mm away from the gingival margins of the upper teeth. The donor site will be closed with a gelatin sponge + cyanoacrylate + suspending sutures.
gelatin sponge + cyanoacrylate + suspending sutures + coconut oil
ACTIVE COMPARATORAfter local anesthesia (2% articaine hydrochloride with epinephrine 1:100,000) administration, palatal thickness will be measured by perpendicularly inserting a Michigan-O periodontal probe from the corners of the rectangular donor area and the mean value will be recorded as palatal tissue thickness. The epithelialized gingival graft will be harvested using 15 knives. After a rectangular-shaped initial incision, a graft with 1-1.5 mm thickness will be harvested approximately 1.5 to 3 mm away from the gingival margins of the upper teeth. The donor site will be closed with a gelatin sponge, cyanoacrylate suspending sutures and coconut oil.
Interventions
The donor site will be closed both with gelatin sponge +Cyanoacrylate (Spongostan®, Ethicon, USA)+ supporting sutures (control group)
Seconder The donor site will be closed both with gelatin sponge +Cyanoacrylate (Spongostan®, USA) and coconut oil (test group)
Eligibility Criteria
You may qualify if:
- age ≥18; mucogingival surgical treatment indication that needs connective tissue graft in the anterior mandible; stable periodontium after phase I therapy; full-mouth plaque and bleeding scores \<15%
You may not qualify if:
- previous palatal harvesting history; unstable endodontic conditions; tooth mobility at the surgical site; systemic disease; pregnancy; use of medications with potential adverse effects on periodontal tissues
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul Medipol University
Istanbul, Fatih, Turkey (Türkiye)
Related Publications (1)
Yilmaz M, Balci N, Gunay B, Parlak HM, Parmaksiz A, Toygar H, Keceli HG. Palatal donor site management using tissue adhesives with adjunctive coconut oil in a randomized clinical trial. Sci Rep. 2025 Aug 26;15(1):31495. doi: 10.1038/s41598-025-17071-5.
PMID: 40858855DERIVED
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- DDs, PhD
Study Record Dates
First Submitted
September 1, 2024
First Posted
September 3, 2024
Study Start
October 10, 2023
Primary Completion
May 20, 2024
Study Completion
May 20, 2024
Last Updated
September 3, 2024
Record last verified: 2024-09
Data Sharing
- IPD Sharing
- Will not share