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Clinical Trial

Tissue Adhesive Versus Sutures in Oral Biopsy Closure

NCT: NCT07654166 · RECRUITING

NCT IDNCT07654166
StatusRECRUITING
Start Date2025-08-12
Completion2027-12
SponsorDamascus University (OTHER)
First posted
Last updated

Brief Summary

Excisional biopsies are commonly performed in the oral mucosa, and proper wound closure and hemostasis are critical for the success of the surgical procedure. Suturing remains the gold standard for closing surgical incisions; however, it has several drawbacks, including being time-consuming and requiring technical skill for proper placement. In addition, access to posterior areas of the oral cavity can be challenging. Suturing may also cause patient discomfort during needle penetration of tissues and can serve as a potential pathway for microbial contamination. Therefore, this randomized controlled clinical trial aims to evaluate one of the latest tissue adhesives from the cyanoacrylate group (PeriAcryl 90 HV) compared to conventional surgical sutures (Nylon 4-0) for wound closure following oral excisional biopsies. A total of 28 patients with oral fibroma will be randomly assigned to either the tissue adhesive group or the suture group (14 patients per group).

Frequently Asked Questions

What is Tissue Adhesive Versus Sutures in Oral Biopsy Closure?

Tissue Adhesive Versus Sutures in Oral Biopsy Closure is a clinical trial registered under NCT07654166. Current status: RECRUITING.

What is the status of NCT07654166?

The current status of NCT07654166 (Tissue Adhesive Versus Sutures in Oral Biopsy Closure) is: RECRUITING.

When did Tissue Adhesive Versus Sutures in Oral Biopsy Closure start?

Tissue Adhesive Versus Sutures in Oral Biopsy Closure started on 2025-08-12.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.