Status:

UNKNOWN

Effect of Suture Material on Postoperative Nipple Areolar Complex Widening

Lead Sponsor:

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Conditions:

Breast Cancer

Gynecomastia

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

This will be a single-blinded study where participants are blinded to the suture type but the surgeon will draw a random, unmarked envelope containing the designated suture type at the start of the su...

Detailed Description

This will be a single-blinded study where the participants will be blinded to the type of suture. The patient population will be all patients undergoing breast surgery at the London Health Sciences Ce...

Eligibility Criteria

Inclusion

  • Any individual undergoing breast surgery of any kind using a periareolar approach including breast reconstruction, mastopexy, mammoplasty gender affirming surgery, mastectomy, or gynecomastia surgery
  • Patients undergoing breast surgery at the London Health Sciences Center (LHSC) or St Joseph's Hospital (SJH)
  • Participants over the age of 18
  • Any BMI
  • Any gender
  • Patients who are willing to participate in the study and provide informed consent.

Exclusion

  • Patient does not or cannot consent for enrollment in this study (includes inability to understand the provided information due to illiteracy or unproficiency in English)
  • Patient is under the age of 18
  • Patients with a known allergy to any type of suture material used in the study.
  • For cancer patients who received radiotherapy, the irradiated breast will not be included in the study (the non-irradiated breast remains eligible)

Key Trial Info

Start Date :

December 1 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

November 1 2024

Estimated Enrollment :

180 Patients enrolled

Trial Details

Trial ID

NCT06070324

Start Date

December 1 2023

End Date

November 1 2024

Last Update

October 6 2023

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