Effectiveness of Meshed Free Gingival Graft for Widening of Keratinized Tissues

NCT ID: NCT06037694

Last Updated: 2025-08-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-01

Study Completion Date

2026-08-01

Brief Summary

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The overall objective of this project is to evaluate, over a period of 1 year, the outcomes of either conventional free gingival graft (FGG) or mesh-FGG to increase the width of keratinized mucosa (KM) at implant sites.

Detailed Description

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The importance of the width of keratinized mucosa (KM) at implant sites remains a subject of ongoing debate. Reduced dimensions of KM (width \<2 mm) are associated with mucosal recession, biofilm accumulation, soft-tissue inflammation, marginal bone loss, peri-implantitis and patient discomfort. Surgical options to increase the width of KM include an apically positioned flap, either alone or in combination with an autogenous graft or a xenogeneic collagen matrix. The free gingival graft (FGG) is a well-established technique with a history of successful clinical use. The harvesting procedure for autogenous graft from the palatal mucosa, however, is usually associated with significant patient morbidity, especially when there is a need to graft extensive mucosal areas. To overcome this problem, various graft modifications have been proposed to limit the need for large-area autografts. Examples include the accordion technique, the strip gingival autograft technique, and a vertical modification of the strip gingival graft. The expanded mesh graft, another graft modification, has been used in the field of plastic surgery, especially in the treatment of large burn wounds. Recently, De Greef, Carcuac, De Mars et al. proposed this technique to be used in periodontal plastic surgery, more specifically, in the widening of KM at implant sites by means of a meshed free gingival graft (mesh-FGG). In this case series, initially inadequate width of KM in edentulous areas could be successfully increased prior to implant installation, without the need for any extensive autograft harvesting. Data from trials comparing mesh-FGG to conventional FGG and assessing the long-term efficacy of this novel technique, however, are missing.

The investigators hypothesize that the mesh-FGG technique will demonstrate similar clinical results (non-inferiority: increase in KM width) but improved patient-reported outcomes (superiority: post-surgical morbidity) compared to the FGG.

Conditions

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Gingiva Atrophy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Free Gingival Graft

A mucogingival surgery where a conventional free gingival graft harvested from the palate is placed on a recipient site prepared to increase the width of KM at implant sites.

Group Type ACTIVE_COMPARATOR

Conventional Free Gingival Graft

Intervention Type PROCEDURE

Implant site with insufficient dimensions of KM will be covered by a conventional free gingival graft.

Meshed Free Gingival Graft

A mucogingival surgery where a meshed free gingival graft harvested from the palate is placed on a recipient site prepared to increase the width of KM at implant sites.

Group Type EXPERIMENTAL

'Mesh Free Gingival Graft

Intervention Type PROCEDURE

Implant site with insufficient dimensions of KM will be covered by a expanded meshed free gingival graft.

Interventions

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Conventional Free Gingival Graft

Implant site with insufficient dimensions of KM will be covered by a conventional free gingival graft.

Intervention Type PROCEDURE

'Mesh Free Gingival Graft

Implant site with insufficient dimensions of KM will be covered by a expanded meshed free gingival graft.

Intervention Type PROCEDURE

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Göteborg University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jan Derks

Role: STUDY_CHAIR

Goteborg University

Locations

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ConfiDent ® Dental Surgery Clinic, Dubai Palm Jumeirah

Dubai, Dubai, United Arab Emirates

Site Status RECRUITING

Countries

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United Arab Emirates

Central Contacts

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Olivier Carcuac, DDS, PhD

Role: CONTACT

556275575 ext. 00971

Jan Derks, DDS, PhD

Role: CONTACT

317863124 ext. 0046

Facility Contacts

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Olivier Carcuac, DDS, PhD

Role: primary

0097556275575

References

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Schwarz F, Derks J, Monje A, Wang HL. Peri-implantitis. J Clin Periodontol. 2018 Jun;45 Suppl 20:S246-S266. doi: 10.1111/jcpe.12954.

Reference Type BACKGROUND
PMID: 29926484 (View on PubMed)

Sanz M, Schwarz F, Herrera D, McClain P, Figuero E, Molina A, Monje A, Montero E, Pascual A, Ramanauskaite A, Renouard F, Sader R, Schiegnitz E, Urban I, Heitz-Mayfield L. Importance of keratinized mucosa around dental implants: Consensus report of group 1 of the DGI/SEPA/Osteology Workshop. Clin Oral Implants Res. 2022 Jun;33 Suppl 23:47-55. doi: 10.1111/clr.13956.

Reference Type BACKGROUND
PMID: 35763021 (View on PubMed)

Lim HC, An SC, Lee DW. A retrospective comparison of three modalities for vestibuloplasty in the posterior mandible: apically positioned flap only vs. free gingival graft vs. collagen matrix. Clin Oral Investig. 2018 Jun;22(5):2121-2128. doi: 10.1007/s00784-017-2320-y. Epub 2017 Dec 23.

Reference Type BACKGROUND
PMID: 29275490 (View on PubMed)

Tavelli L, Barootchi S, Avila-Ortiz G, Urban IA, Giannobile WV, Wang HL. Peri-implant soft tissue phenotype modification and its impact on peri-implant health: A systematic review and network meta-analysis. J Periodontol. 2021 Jan;92(1):21-44. doi: 10.1002/JPER.19-0716. Epub 2020 Aug 9.

Reference Type BACKGROUND
PMID: 32710810 (View on PubMed)

Singh M, Nuutila K, Collins KC, Huang A. Evolution of skin grafting for treatment of burns: Reverdin pinch grafting to Tanner mesh grafting and beyond. Burns. 2017 Sep;43(6):1149-1154. doi: 10.1016/j.burns.2017.01.015. Epub 2017 Jan 30.

Reference Type BACKGROUND
PMID: 28153583 (View on PubMed)

De Greef A, Carcuac O, De Mars G, Stankov V, Cortasse B, Giordani G, Van Dooren E. The expanded mesh free gingival graft: A novel approach to increase the width of keratinized mucosa. Clin Adv Periodontics. 2024 Sep;14(3):157-164. doi: 10.1002/cap.10264. Epub 2023 Aug 16.

Reference Type BACKGROUND
PMID: 37551510 (View on PubMed)

Thoma DS, Naenni N, Figuero E, Hammerle CHF, Schwarz F, Jung RE, Sanz-Sanchez I. Effects of soft tissue augmentation procedures on peri-implant health or disease: A systematic review and meta-analysis. Clin Oral Implants Res. 2018 Mar;29 Suppl 15:32-49. doi: 10.1111/clr.13114.

Reference Type BACKGROUND
PMID: 29498129 (View on PubMed)

Other Identifiers

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OCarcuac-meshFGG

Identifier Type: -

Identifier Source: org_study_id

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