Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06614829

Patient Reported Experiences and Outcomes Associated with Standard C-Section Wound Closure Versus STRATAFIX/DERMABOND PRINEO Wound Closure (CS-PREO)

Led by North York General Hospital · Updated on 2024-11-29

68

Participants Needed

1

Research Sites

57 weeks

Total Duration

On this page

Sponsors

N

North York General Hospital

Lead Sponsor

J

Johnson & Johnson

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of the study is to compare outcomes between patients receiving standard C-section wound closure compared to a wound closure bundle that includes Stratafix sutures and Dermabond PRINEO.

CONDITIONS

Official Title

Patient Reported Experiences and Outcomes Associated with Standard C-Section Wound Closure Versus STRATAFIX/DERMABOND PRINEO Wound Closure (CS-PREO)

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient must be 18 years of age or older at time of recruitment
  • Patients opting for a planned (elective) C-Section between 13 and 36 weeks gestation are eligible
  • Patients must have internet access and/or a smartphone to complete study questionnaires
  • Patients must be able to speak and write in English as questionnaires are only in English
  • Patients must have coverage from the Ontario Health Insurance Plan (OHIP)
Not Eligible

You will not qualify if you...

  • Patients with conditions assessed by the surgeon that may affect ability to consent or use the virtual care platform (e.g., intellectual disabilities)
  • Patients expected to have significant maternal complications affecting the surgery
  • Patients who have an unplanned emergency C-section after enrollment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

North York General Hospital

North York, Ontario, Canada, M2K1E1

Actively Recruiting

Loading map...

Research Team

M

Mark Fan, MHSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here