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to Compare the Cosmetic Outcome Using Dermabond Tissue Glue vs Subcuticular Suture in Neck Surgeries

Randomised Controlled Trial to Compare the Cosmetic Outcome Using Dermabond Tissue Glue vs Subcuticular Suture in Neck Surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047373
Enrollment
30
Registered
2022-11-16
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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: DERMABOND: Patient group in which dermabond tissue glue is being applied to close the neck wound. Control Intervention1: MONOCRYL: Patients group in whom monocryl sutures are applied to

Sponsors

PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All patients undergoing thyroid and parathyroid surgery 2. Age 18-60 years. 3. Any gender. 4. Acceptance of the study by the patient by a valid informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients who had a history of allergies to cyanoacrylate products. 2. Patients who have received radiotherapy in head and neck region before surgery 3. Patients with collagen vascular diseases. 4. Patients requiring revision surgery.

Design outcomes

Primary

MeasureTime frame
To assess the cosmetic outcome between subcuticular closure and dermabond tissue glue closure using POSAS scaleTimepoint: At 6 weeks and 3 months post operatively—

Secondary

MeasureTime frame
To assess the incidence of surgical site infection with two techniques.Timepoint: Within 30 days post operatively—

Countries

India

Contacts

Public ContactProf Divya Dahiya

Post Graduate Institute of Medical Education and Research

dahiyadivya@yahoo.com7087008131

Outcome results

None listed

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