Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Free Gingival Graft Patients' Treatment Perception and Experience

8. juni 2026 oppdatert av: Cenker Zeki Koyuncuoğlu, Istanbul Aydın University

Patient Experience and Treatment Perception in Patients Undergoing Free Gingival Graft: A Retrospective Survey Study.

Free gingival graft (FGG) is a common and effective periodontal procedure used to improve gum health; however, it can involve challenges such as postoperative pain and discomfort due to the requirement of a secondary donor site. While clinical outcomes are well-documented, long-term patient perceptions and overall satisfaction levels have not been sufficiently explored. The purpose of this retrospective study is to systematically evaluate patient experiences, satisfaction levels, and the willingness to undergo the procedure again in individuals who underwent FGG surgery at least one year ago.

Studieoversikt

Detaljert beskrivelse

Background and Rationale: Free gingival graft (FGG) is a widely preferred mucogingival procedure in periodontal plastic surgery, aimed at increasing keratinized tissue width and improving gingival morphology. While FGG is highly effective for indications such as preventing gingival recession and enhancing oral hygiene maintenance, it requires a secondary surgical site (donor area), which can lead to postoperative pain, tissue morbidity, and reduced patient comfort. Current literature often focuses on short-term clinical outcomes, leaving long-term patient-reported outcome measures (PROMs) and perceptions insufficiently explored.

Objectives:The primary objective of this study is to retrospectively evaluate the postoperative experiences, satisfaction levels, and overall surgical perceptions of individuals who underwent FGG surgery. Specifically, the study aims to investigate the willingness of patients to undergo the procedure again, should it be necessary in the future.

Methodology: This is a retrospective, non-interventional, observational, and cross-sectional study conducted at Istanbul Aydin University, Faculty of Dentistry, Department of Periodontology. The study population includes patients who underwent FGG surgery between January 2014 and May 2024, with at least one year having passed since the operation.Data collection involves two stages:

  1. Archive Review: Patient demographics, smoking status, systemic health, and surgical details (e.g., complications, donor site technique) are retrieved from institutional records.
  2. Telephone Survey: A semi-structured survey is administered via telephone to assess patient-reported outcomes, including pain levels, satisfaction, analgesic requirements, and aesthetic perceptions.

Studietype

Observasjonsmessig

Registrering (Faktiske)

77

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Turkey
      • Istanbul, Turkey, Tyrkia (Türkiye), 34295
        • Istanbul Aydin University, Faculty of Dentistry, Department of Periodontology

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

The study population consists of patients who underwent Free Gingival Graft (FGG) surgery at the Department of Periodontology, Faculty of Dentistry, Istanbul Aydın University, between January 2014 and May 2024. Potential participants were identified through a retrospective screening of institutional archive records based on the predefined inclusion and exclusion criteria

Beskrivelse

Inclusion Criteria:

  • Individuals who underwent Free Gingival Graft (FGG) surgery at Istanbul Aydin University, Faculty of Dentistry, Department of Periodontology; who accurately remember the surgical site and grant permission to use their patient records containing demographic and surgical data.
  • Patients who have undergone periodontal plastic surgery due to an FGG procedure only once.
  • Patients whose records contain complete information regarding the graft harvesting technique from the palatal donor site, including the date of the procedure and any complications within the first month following surgery.
  • Patients who have not previously undergone any other surgical procedure in the palatal region.

Exclusion Criteria:

  • Individuals who have not undergone FGG surgery.
  • Patients who have undergone periodontal plastic surgery more than once.
  • Patients who underwent FGG surgery but have missing or incomplete information in their medical records.
  • Patients who have previously undergone any other surgical procedure in the palatal region.
  • Patients who have previously received a different periodontal surgical treatment in the area where the relevant teeth are located.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
Free Gingival Graft Patients
Patients who underwent free gingival graft (FGG) surgery at the Department of Periodontology, Faculty of Dentistry, Istanbul Aydın University, between January 2014 and May 2024
A surgical procedure performed to increase the amount of keratinised gingival tissue and improve periodontal health. The study examines the postoperative experiences and satisfaction levels of patients who have undergone this procedure.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Patient Satisfaction and Willingness to Undergo the Procedure Again
Tidsramme: At least 1 year post-operation (Range: 1 to 11 years, based on surgeries performed between January 2014 and May 2024).
This measure evaluates the overall satisfaction of patients who underwent Free Gingival Graft (FGG) surgery and their willingness to repeat the procedure if necessary in the future. The assessment is conducted through a semi-structured retrospective telephone survey that covers postoperative pain, complications, aesthetic perception, and overall treatment experience.
At least 1 year post-operation (Range: 1 to 11 years, based on surgeries performed between January 2014 and May 2024).

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

27. juni 2025

Primær fullføring (Faktiske)

30. september 2025

Studiet fullført (Faktiske)

30. september 2025

Datoer for studieregistrering

Først innsendt

28. april 2026

Først innsendt som oppfylte QC-kriteriene

28. april 2026

Først lagt ut (Faktiske)

5. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

8. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

As the informed consent form guarantees participants that their data will not be shared with third parties, the data will not be made available for sharing.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere