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TERMINATED
NCT06593275
NA

Flowable Resin Versus Self-Adhesive Dressing for Palatal Donor-Site Protection

Sponsor: Universidad de Especialidades Espiritu Santo

View on ClinicalTrials.gov

Summary

This pilot randomized clinical study compared two methods for protecting the palatal donor site after harvesting a free gingival graft. Twelve adult participants were randomly assigned to receive either a hemostatic collagen sponge covered with flowable resin composite or a hemostatic collagen sponge covered with a self-adhesive oral dressing stabilized with sutures. Participants recorded pain at the palatal donor site daily for 14 days using a 0-to-10 pain scale. The study also evaluated the time required to apply each protective material and the number of days that it remained in place.

Official title: Flowable Resin Composite Versus a Self-Adhesive Oral Dressing for Palatal Donor-Site Protection After Free Gingival Graft Harvesting: A Pilot Randomized Clinical Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

12

Start Date

2023-10-30

Completion Date

2025-03-01

Last Updated

2026-10-23

Healthy Volunteers

No

Interventions

DEVICE

Flowable Resin Composite Palatal Barrier

A hemostatic collagen sponge was covered by a light-cured flowable resin composite barrier bonded to the palatal enamel surfaces of the adjacent teeth.

DEVICE

Self-Adhesive Oral Dressing

A hemostatic collagen sponge was covered by a self-adhesive oral dressing stabilized with X-shaped 5-0 nylon sutures.

Locations (1)

Universidad de Especialidades Espiritu Santo

Samborondón, Guayas, Ecuador