Viewing Study NCT06509165



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Last Modification Date: 2024-10-26 @ 3:35 PM
Study NCT ID: NCT06509165
Status: COMPLETED
Last Update Posted: None
First Post: 2024-07-08

Brief Title: Comparison of Different Techniques in the Treatment of Gingival Recession
Sponsor: None
Organization: None

Study Overview

Official Title: Comparison of Clinical and Aesthetic Results of Different Techniques in the Treatment of Gingival Recession
Status: COMPLETED
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of this study is to compare the clinical and aesthetic results of different techniques in the treatment of gingival recession

The main questions it aims to answer are

Does the surgical technique preferred by the physician affect the closure rate of gingival recession in the 3rd month
Does the surgical technique preferred by the physician affect the closure rate of gingival recession in the 6th month Participants were informed about the study Following routine periodontal treatment surgical operations were performed on the areas with receding gums using different techniques for the patients included in the study
Detailed Description: After the routine clinical and radiological periodontal evaluation of every patient applying to the periodontology department phase-I periodontal treatment is first applied to every patient diagnosed with periodontal disease Patients are then given the necessary information to ensure plaque control Gingival recessions that make mechanical cleaning of the patient difficult and the dentine sensitivity reported by the patient due to these recessions make plaque control difficult for the patient It is routinely applied to patients who are found to have gingival recessions that cause these problems These applications vary depending on the withdrawal type

In patients with gingival recession who apply to the periodontology department gingival recession closure operations performed with subepithelial connective tissue graft laterally placed flap coronally placed flap modified coronally placed flap tunnel technique vestibular incision and subperiosteal tunnel access technique are preferred The change and recovery status of the patients after the treatments are evaluated and followed up with routine photographs

Photographs of the procedures and the wound area during and after the operations are taken and stored in the clinic photo archive

Objective success after root closure procedures is monitored with clinical records and measurements at regular intervals Success after root closure is evaluated in two categories clinical and aesthetic success Clinical success The reduction in withdrawal depth is determined by measuring clinical binding gain To determine these clinical measurements of the patients at the beginning 1st month 3rd month 6th month and 12th month are recorded and photographs are taken At the same time since there are other factors that affect both aesthetic and clinical success the type of recession aesthetic complaints sensitivity and brushing effectiveness are recorded before and after treatment For this reason the amount of recession keratinized tissue mm clinical attachment level plaque index pocket depth papilla width and height values are recorded and compared in the initial and follow-up examinations of the patients

Individual choice

For this study patients who receive gingival recession treatment at the Periodontology clinic and those who agree to take routine photographs before and after treatment and who sign the consent form if they meet the inclusion criteria for the study will be included in the study Our study is a retrospective study Clinical and photographic records of patients who had previous gingival recession surgery by a clinician at the periodontology clinic will be used in the study

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None