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Vertical Scar Versus Inferior Pedicle Reduction Mammoplasty

Primary Purpose

Breast Hypertrophy

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Vertical scar versus inferior pedicle reduction mammoplasty
Sponsored by
McMaster University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Hypertrophy focused on measuring cost-utility analysis;, breast reduction;, vertical scar mammoplasty;, pedicle reduction mammoplasty

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Patients suffering from breast hypertrophy Patients who received OHIP approval for reduction mammoplasty Candidate for both surgical procedures Patient is willing to complete quality of life questionnaires and follow up Patient will provide informed consent Exclusion Criteria: Unilateral Breast Hypertrophy Patients under the age of 18 years Inability to complete questionnaires due to language problems Bilateral mastopexy (breast lift) Previous breast reduction surgery Patients who will require greater than 1000 grams to be removed from either breast (to be assessed by the Archimedes principle* preoperatively; patients who by the Archimedes principle displace 1400 cc of volume will be excluded from the study) Pre-operative radiation after lumpectomy If another procedure is to be "piggy backed' to the reduction mammoplasty (e.g. liposuction to breast or elsewhere, abdominoplasty, etc) The Archimedes principle is as follows: In the privacy of her bathroom the patient will immerse each breast separately into a large pot filled to the brim with tap water. The breast will displace some of the water which will be collected into another larger container e.g. plastic dish pan placed underneath the pot. The patient will be asked to measure the volume of the displaced water in ml. The volume that will be displaced will approximate the weight of the breast. The measurement will be done 3 times and the average for each breast will be recorded. (The surgeon will explain this principle only to those patients where there is uncertainty whether the resection will exceed 1000 grams. For the rest of the patients this is not necessary.)

Sites / Locations

  • St. Joseph's Healthcare

Outcomes

Primary Outcome Measures

Health related quality of life (utilities and disease specific)

Secondary Outcome Measures

Health care resource utilization as well as out-of-pocket expenses by patients and caregivers.

Full Information

First Posted
September 6, 2005
Last Updated
July 27, 2011
Sponsor
McMaster University
Collaborators
Canadian Society of Plastic Surgeons
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1. Study Identification

Unique Protocol Identification Number
NCT00149344
Brief Title
Vertical Scar Versus Inferior Pedicle Reduction Mammoplasty
Official Title
Vertical Scar Versus Inferior Pedicle Reduction Mammoplasty: A Randomized Controlled Trial and Cost-Utility Analysis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2011
Overall Recruitment Status
Completed
Study Start Date
September 2005 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
July 2011 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
McMaster University
Collaborators
Canadian Society of Plastic Surgeons

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Main research question: Is vertical scar reduction mammoplasty superior when compared to inferior pedicle reduction mammoplasty in terms of patient quality of life and cost-effectiveness? Why is this research important?: There is on-going controversy among plastic surgeons as to the superiority of one technique (vertical scar mammoplasty versus inferior pedicle reduction mammoplasty) over the other in terms of patient health related quality of life and health care resource utilization. What is being studied?: We are studying (comparing) two surgical procedures for breast reduction mammoplasty (vertical scar mammoplasty versus inferior pedicle reduction mammoplasty).
Detailed Description
Breast reduction is one of the most common procedures performed by plastic surgeons. Because it is common and in most jurisdictions requires at least one day of hospital stay, it consumes considerable health care resources. Although multiple techniques have been reported, the two top competing techniques used in North America are the inferior pedicle technique and the vertical scar technique. There is on-going controversy as to the superiority of one technique over the other in terms of patient satisfaction and health care resource utilization. In the last few years, third party payers have been concerned with the unnecessary consumption of scarce health care resources due to the variation of practice mostly influenced by surgeon preferences rather than valid evidence. The purpose of this study is to test the hypothesis that Vertical Scar Reduction Mammoplasty (VSR) is superior to the Inferior Pedicle Reduction Mammoplasty (IPR) in terms of patient health-related quality of life (HRQL). Health related quality of life will be measured by the Health Utilities Index Mark 2/3 (HUI) providing the outcome, quality adjusted life years (QALYs) and the Breast Reduction Assessment Value and Outcomes (BRAVO) instruments. The BRAVO instruments consist of a set of separate instruments including the Short Form 36 (SF-36), the Multidimensional Body Self Relations Questionnaire Appearance Assessment (MBSRQ-AS), and the Breast Related Symptoms Questionnaire (BRSQ). The MBSRQ-AS provides a measure of self-evaluation of appearance, and the BRSQ measures the breast symptom score. Secondly, we will test whether the VSR is a more cost-effective procedure. If the hypothesis is confirmed that the VSR technique is more cost-effective, then there will be compelling evidence to adopt it. Regardless of whether VSR is found to be cost-effective, the plastic surgery community, third party payers, and patients will be informed about the results.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Hypertrophy
Keywords
cost-utility analysis;, breast reduction;, vertical scar mammoplasty;, pedicle reduction mammoplasty

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
254 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Radiation
Intervention Name(s)
Vertical scar versus inferior pedicle reduction mammoplasty
Intervention Description
Vertical Scar Reduction Mammoplasty Inferior Pedicle Reduction Mammoplasty
Primary Outcome Measure Information:
Title
Health related quality of life (utilities and disease specific)
Time Frame
1 Year
Secondary Outcome Measure Information:
Title
Health care resource utilization as well as out-of-pocket expenses by patients and caregivers.
Time Frame
1 Year

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients suffering from breast hypertrophy Patients who received OHIP approval for reduction mammoplasty Candidate for both surgical procedures Patient is willing to complete quality of life questionnaires and follow up Patient will provide informed consent Exclusion Criteria: Unilateral Breast Hypertrophy Patients under the age of 18 years Inability to complete questionnaires due to language problems Bilateral mastopexy (breast lift) Previous breast reduction surgery Patients who will require greater than 1000 grams to be removed from either breast (to be assessed by the Archimedes principle* preoperatively; patients who by the Archimedes principle displace 1400 cc of volume will be excluded from the study) Pre-operative radiation after lumpectomy If another procedure is to be "piggy backed' to the reduction mammoplasty (e.g. liposuction to breast or elsewhere, abdominoplasty, etc) The Archimedes principle is as follows: In the privacy of her bathroom the patient will immerse each breast separately into a large pot filled to the brim with tap water. The breast will displace some of the water which will be collected into another larger container e.g. plastic dish pan placed underneath the pot. The patient will be asked to measure the volume of the displaced water in ml. The volume that will be displaced will approximate the weight of the breast. The measurement will be done 3 times and the average for each breast will be recorded. (The surgeon will explain this principle only to those patients where there is uncertainty whether the resection will exceed 1000 grams. For the rest of the patients this is not necessary.)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Achilleas Thoma, MD MSc FRCSC
Organizational Affiliation
McMaster University / St. Joseph's Healthcare
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Joseph's Healthcare
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 4A6
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
25255113
Citation
Thoma A, Kaur MN, Tsoi B, Ziolkowski N, Duku E, Goldsmith CH. Cost-effectiveness analysis parallel to a randomized controlled trial comparing vertical scar reduction and inverted T-shaped reduction mammaplasty. Plast Reconstr Surg. 2014 Dec;134(6):1093-1107. doi: 10.1097/PRS.0000000000000751.
Results Reference
derived

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Vertical Scar Versus Inferior Pedicle Reduction Mammoplasty

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