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A study to compare the appearance of scar after using either tissue glue or stitches for closing facial surgery wound

Comparative Evaluation of the Esthetic Outcomes of Octyl 2 Cyanoacrylate Skin Adhesive and Ethilon Suture in Patients requiring Skin Incisions in Maxillofacial Surgery: A Randomized Clinical Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/11/022020
Enrollment
20
Registered
2019-11-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Octyl 2 Cyanoacrylate: Skin closure using dermabond which flakes off in 7 - 10 days Control Intervention1: Ethilon Sutures: Skin closure using 4-0 Ethilon sutures that will be removed a

Sponsors

Department of Oral Maxillofacial Surgery
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients between age group 15-50 years. 2. Patients both males and females will be included. 3. Clean elective extra-oral surgical incisions. 4. Patients who would require retromandibular or submandibular surgical incisions. 5. Extra-oral surgical incision length 2-8cm. 6. Incision with good approximation of edges where closure would not be under tension. 7. Patient willingness for study and follow up.

Exclusion criteria

Exclusion criteria: 1. Patients with systemic conditions impairing wound healing (uncontrolled diabetes mellitus, vascular problems, coagulation disorders, peripheral vascular disorders). 2. Patients on immunomodulators (steroids, cyclosporine). 3. Patients with known tendency of hypertrophic scar or keloid formation. 4. Extra-oral surgical wounds in the region of malignancy. 5. Extra-oral surgical wounds in the region of mucocutaneous junction, periocular region. 6. Extra-oral surgical wounds in the region where there is visual evidence of active infection, rash or skin lesions. 7. Extra-oral surgical wounds in the region covered by natural hair. 8. Patients with known history of hypersensitivity to formaldehyde or cyanoacrylates. 9. Uncooperative patients and mentally retarded patients.

Design outcomes

Primary

MeasureTime frame
To evaluate the esthetic results achieved using octyl-2-cyanoacrylate skin adhesive and ethilon suture in patients requiring skin incisions in maxillofacial surgeryTimepoint: End of 1st and 3rd post-operative month

Secondary

MeasureTime frame
Compare the time taken for skin closure achieved using octyl-2-cyanoacrylate skin adhesive and ethilon suture in patients requiring skin incisions in maxillofacial surgeryTimepoint: at the time of closure;Observe tissue response and incidence of complications involved with the use of octyl-2-cyanoacrylate skin adhesive and ethilon suture in patients requiring skin incisions in maxillofacial surgeryTimepoint: 7th, 15th day and 1st month post-operatively

Countries

India

Contacts

Public ContactDr Srivalli Natarajan

MGM Dental College and Hospital

drushaasnani@gmail.com9820897181

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026