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Trial Investigating Cyanoacrylate Glue to Prevent Surgical Site Infection Following Breast Surgery

Trial Investigating Cyanoacrylate Glue to Prevent Surgical Site Infection Following Breast Surgery

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02779296
Enrollment
30
Registered
2016-05-20
Start date
2016-06-30
Completion date
Unknown
Last updated
2016-05-20

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

Conditions

Surgical Wound Infection

Keywords

Cyanoacrylates, Mammaplasty, Mastectomy

Brief summary

Surgical Site Infections (SSI) represents a significant complication in plastic surgery. Infections can result in a prolonged recovery and impair long-term cosmetic appearance. One potential method to reduce infection is by applying a thin layer of dermal glue over the sutures at the site of incision immediately after the surgery. Conventional closures, such as sutures or staples, leave the site vulnerable until epithelialization occurs in 24 to 48 hours. In contrast, dermal glue provides an instant, waterproof barrier and it has been shown to have intrinsic bacteriostatic properties. The glue is supplied as a liquid enclosed in a vial and when applied, polymerizes rapidly in an exothermic reaction in the presence of moisture to form a solid adhesive. 2-Octylcyanoacrylate (2-OCA)-based glue is formulated to be more flexible than previous preparations. The application of dermal glue is rapid, simple and requires no specific follow-up as it naturally sloughs off overtime. The purpose of this study is to determine if 2-OCA-based glue can reduce the rate of surgical site infection following surgery. Patients undergoing breast surgery will be recruited and randomized to either a group receiving a layer of glue over sutures following surgery or no treatment. Patients will be followed up at 30 days and at 8 months for signs of infection, additional complications and the visual appearance of the scars. The cost of treating and infection will be calculated to determine if using dermal glue to prevent infection is economically feasible. This research has the potential to find a method to reduce surgical site infection, which can be applied to other surgeries.

Interventions

OTHER2-Octyl Cyanoacrylate Glue

topical

Sponsors

Ottawa Hospital Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* patient has provided signed consent * undergoing surgery on the breast

Exclusion criteria

* Infection within 30 days * Previous hypersensitivity to cyanoacrylates or formaldehyde

Design outcomes

Primary

MeasureTime frame
Surgical Site Infection30 days post surgery

Secondary

MeasureTime frameDescription
Other Surgical Complications30 days post surgeryHematoma, seroma, wound dehiscence, scar hyperpigmentation, necrosis (nipple areolar complex, wound edges, fat tissue)
Cosmetic Appearance assessed by the Patient and Observer Scar Assessment Scale (POSAS) v2.030 days post surgery
Cost Analysis to determine the cost to treat a patient with and without a surgical site infection8 months post surgeryThis analysis will be conducted from a Ministry of Health perspective and will factor the additional cost of the glue with the additional cost of treating a surgical site infection (such as antibiotics, additional healthcare visits, treatments and procedures).

Contacts

Primary ContactGloria M Rockwell, MD, MSc
613-737-8899

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026