MedTrace Logo

To Measure Pain Perception Following De-Epithelized Free Gingival Graft Harvesting

NCT03895476 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 72

Last updated 2024-08-23

Study results available
· View outcomes & findings →

Summary

This randomized clinical comparative study will evaluate the postoperative pain following the FGG graft harvest procedure technique covered by four different methods for coverage of the palatal donor site.

Conditions

  • Gingival Recession
  • Palate; Wound

Interventions

DIAGNOSTIC_TEST

palatal wound will be cover with collagen and sutures

after harvesting the graft from the palate, a collagen sponge will be sutured to cover the harvested site

DIAGNOSTIC_TEST

palatal wound covered with platelet rich fibrin

after harvesting the graft from the palate the platelet rich fibrin will be sutured to covered the harvested site

DIAGNOSTIC_TEST

palatal wound covered with a collagen sponge and cyanoacrylate

after harvesting the graft from the palate a collagen sponge will be sealed with cyanoacrylate in position

DIAGNOSTIC_TEST

palatal wound covered with a stent

after harvesting the graft from the palate a stent that will be prepared for the patient, will be placed on to cover the wound

Sponsors & Collaborators

  • University of Alabama at Birmingham

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-06-08
Primary Completion
2021-07-30
Completion
2023-02-27

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03895476 on ClinicalTrials.gov