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Evaluation of use of tissue adhesive in surgeries of wisdom tooth

Evaluation of the use of 2-octyl cyanoacrylate (Dermabond®) adhesive in the closure of the surgical wound in surgery of mandibular third molars

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-108mccss
Enrollment
Unknown
Registered
2023-11-21
Start date
2023-04-10
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Wound Healing

Interventions

A split-mouth study will be carried out, with patients from the Oral and Maxillofacial Surgery and Traumatology Service of UFPR in need of extraction of impacted and/or semi-included lower third molar
D02.241.081.069.366.350
E04.545.700

Sponsors

Universidade Federal do Paraná
Lead Sponsor
Universidade Federal do Paraná
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult individuals of both sexes; Presence of bilateral mandibular third molars in similar positions, according to Winter's classification; Agree to participate in the study

Exclusion criteria

Exclusion criteria: Allergy to any component of Dermabond®; Patients using medications that may interfere with healing (antiplatelet agents, anticoagulants, immunosuppressants, corticoids); Smoking patients; Patients with uncontrolled systemic alterations

Design outcomes

Primary

MeasureTime frame
It is expected to find no difference in healing, postoperative pain, edema and bleeding between the cyanoacrylate tissue adhesive (Dermabond®), evaluated through postoperative questionnaires and facial measurements—

Secondary

MeasureTime frame
No secondary outcomes are expected—

Countries

Brazil

Contacts

Public ContactMarina Fanderuff

Universidade Federal do Paraná

marinafanderuff@hotmail.com55(41) 995270210

Outcome results

None listed

Source: REBEC (via WHO ICTRP)