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Fixation of Free Gingival Graft Using Tissue Tacks vs Criss-cross Sutures

Assessment of Pain Score After Fixation of Free Gingival Graft Using Tissue Tacks Versus Criss- Cross Sutures in Cases With Insufficient Keratinized Tissue. A Randomized Controlled Clinical Trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07823374
Enrollment
16
Registered
2026-09-16
Start date
2025-01-01
Completion date
2026-09-30
Last updated
2026-09-16

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

Conditions

Lack of Keratinized Tissue

Brief summary

Tissue tacks may improve graft stability but their effect on pain is unclear. The study compares tacks and sutures by measuring pain, stability, healing success, and patient comfort.

Detailed description

Tissue tacks are a newer method for securing free gingival grafts ,offering potential benefits such as improved graft stability and reduced movement compared to traditional criss- cross sutures. However, the impact of tissue tacks on postoperative pain remains unclear. This study seeks to evaluate whether tissue tacks, while possibly enhancing graft stability and healing, result in higher pain levels compared to sutures, and whether these outcomes affect the overall clinical success and patient comfort during healing.

Interventions

PROCEDURECriss cross sutures

Fixation of free gingival graft using criss cross sutures

PROCEDURETissue tacs

Fixation of free gingival graft using tissue tacs

Sponsors

October University for Modern Sciences and Arts
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Patients with inadequate keratinized tissue requiring free gingival grafts. * Age between 18-40 years. * Free from systemic diseases that could affect healing. * Good oral hygiene. * Motivated patients with a willingness to participate and comply with post-operative instructions.

Exclusion criteria

* Medically compromised patients * Subjects who underwent radiotherapy or chemotherapy, pregnant women, smokers.

Design outcomes

Primary

MeasureTime frameDescription
Pain score (VAS Score)1,3,5,7 days post surgeryGrade from 1-10

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 17, 2026