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The Role of 2-octyl Cyanoacrylate in Prevention of Recurrent Adhesions After Circumcision

The Role of 2-octyl Cyanoacrylate in Prevention of Recurrent Adhesions After Circumcision

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01794221
Acronym
Circglue
Enrollment
422
Registered
2013-02-18
Start date
2012-11-30
Completion date
2017-09-30
Last updated
2019-01-10

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

Conditions

Adhesions, Phimosis

Keywords

circumcision, 2 octyl cyanoacrylate, phimosis

Brief summary

The objective of this study is to evaluate whether 2-octyl cyanoacrylate skin adhesive decreased the incidence of recurrent adhesions after circumcision. The investigators hypothesize that the incidence of recurrent adhesions will be decreased with use of 2-octyl cyanoacrylate skin adhesive.

Detailed description

The objective of this study is to evaluate whether 2-octyl cyanoacrylate skin adhesive decreased the incidence of recurrent adhesions after circumcision. The investigators hypothesize that the incidence of recurrent adhesions will be decreased with use of 2-octyl cyanoacrylate skin adhesive. Secondary Objective(s) To assess parent satisfaction and comfort level after circumcision with use of 2-octyl cyanoacrylate skin adhesive and compare to those undergoing circumcision without the use of 2-octyl cyanoacrylate skin adhesive.

Interventions

PROCEDUREstitches and skin adhesive

In addition to stitches, 2-octyl cyanoacrylate skin adhesive will be applied to the circumcision wound.

PROCEDUREstitches only

standard of care

Sponsors

Children's Mercy Hospital Kansas City
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
1 Days to 7 Years
Healthy volunteers
No

Inclusion criteria

* All patients undergoing circumcision * Only male patients under the age of 7 years will be eligible

Exclusion criteria

* Any patient over 7 years of age * Previous circumcision * Any parents who are not English language speaking

Design outcomes

Primary

MeasureTime frameDescription
Post circumcision adhesions3-6 weeksEvaluation for adhesions

Secondary

MeasureTime frameDescription
Parent satisfaction and comfort level with circumcision results3-6 weeksParent survey at follow-up visit.

Countries

United States

Outcome results

None listed

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