FindTrial
Sign In

Effect of Two Procedures for Dressing the Roof of the Mouth Evaluating Pain, Quality of Life and Healing in People Who Underwent Gum Grafting

Effect of different protective interventions of the palatal donor area on Healing, Pain and Quality of Life of individuals undergoing Epithelized Free Gingival Grafts: randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-10qgbdg3
Enrollment
Unknown
Registered
2024-04-28
Start date
2024-05-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain Measurement

Interventions

Randomized controlled trial, which seeks to evaluate the effect of three different methods of protecting the donor area in epithelialized free gingival grafts (EGLE) on the healing process, postoperat
E06.892

Sponsors

Universidade Federal de Minas Gerais (UFMG)
Lead Sponsor
Universidade Federal de Minas Gerais (UFMG)
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Individuals aged 18 or over; systemically healthy or controlled American Society of Anesthesiologists (ASA) (ASA I / ASA II); with minimum palatal tissue thickness 2mm assessed with a University of North Carolina (UNC) periodontal probe; both genders

Exclusion criteria

Exclusion criteria: Smokers and alcoholics; individuals with altered coagulation, i.e., history of hemophilia, von Willebrand disease, or currently undergoing anticoagulant therapy; individuals with altered healing patterns, that is, decompensated type 2 Diabetes Mellitus; pregnant and breastfeeding women; individuals with a history of bacterial endocarditis; with continuous use of anti-inflammatories and corticosteroids; individuals who underwent gum grafting in the last 6 months

Design outcomes

Primary

MeasureTime frame
It is expected to find a statistically relevant reduction in self-reported post-operative pain by individuals in the test groups, verified through the application of the analogue pain scale (VAS) after 15 days of the surgical procedure.—

Secondary

MeasureTime frame
It is expected to find an improvement in the quality of life of individuals undergoing the surgical procedure in the test groups in relation to the control group, through the application of the Oral Health Impact Profile (OHIP-14) instrument, before and 15 days after surgery;It is expected to find an improvement in the healing process of the palatal wound of individuals undergoing the surgical procedure in the test groups in relation to the control group, through visual verification through photographs, before and 15 days after the procedure. Using visualization scores of fibrin points in the wound. In addition to investigating the palatal scarring process through the topical application of hydrogen peroxide at the wound site and visualization of the bubbling process or not at the site, before and after 15 days of the surgical procedure—

Countries

Brazil

Contacts

Public ContactLucas Padovani

Universidade Federal de Minas Gerais - UFMG

lpadovani@ufmg.br+55(31)34092470

Outcome results

None listed

Source: REBEC (via WHO ICTRP)