Using meshed free gingival grafts to improve gum tissue width
Widening of Keratinized Tissues With an Expanded Meshed Free Gingival Graft: a Multi-center Randomized Controlled Trial.
This study is testing whether a new way of grafting gum tissue can help people with thin gums around dental implants feel more comfortable and have better results than the traditional method.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | Göteborg University Academic / other |
| Locations | 1 site (Dubai, Dubai) |
| Trial ID | NCT06037694 on ClinicalTrials.gov |
What this trial studies
This project aims to evaluate the effectiveness of two techniques, conventional free gingival graft (FGG) and meshed free gingival graft (mesh-FGG), in increasing the width of keratinized mucosa at implant sites over a one-year period. The study addresses the issue of gingiva atrophy, which can lead to various complications such as mucosal recession and peri-implantitis. By comparing these two grafting methods, the researchers hope to determine which approach provides better outcomes with less patient morbidity. The study will include patients with inadequate keratinized mucosa and discomfort related to oral hygiene.
Who should consider this trial
Good fit: Ideal candidates are systemically healthy adults aged 18 and older with inadequate keratinized mucosa around adjacent dental implants.
Not a fit: Patients who are pregnant, lactating, smokers, or have uncontrolled medical conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a less invasive and more effective method for improving gum tissue health around dental implants.
How similar studies have performed: Previous studies have shown promising results with similar grafting techniques in periodontal plastic surgery, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ≥18 years of age, * systemically healthy, * presence of ≥2 adjacent implants in both sides of the mandibles showing \<2 mm of KM on the buccal aspects, * subjects have to present with discomfort from brushing and/or difficulties in maintaining proper home care due to inadequate dimension of KM * Full-Mouth Plaque Score (FMPS) \<20%, * Full-Mouth Bleeding Score (FMBS) \<20%. Exclusion Criteria: * pregnancy or lactation, * tobacco smoking, * uncontrolled medical condition, * medication that can affect gingival conditions.
Where this trial is running
Dubai, Dubai
- ConfiDent ® Dental Surgery Clinic, Dubai Palm Jumeirah — Dubai, Dubai, United Arab Emirates (Recruiting)
Study contacts
- Study coordinator: Olivier Carcuac, DDS, PhD
- Email: olivier.carcuac@gu.se
- Phone: 556275575
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.