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Clinical Trials/NCT01857765
NCT01857765
Withdrawn
N/A

How Rehabilitation Affects the Time to Pain-free Living After Endoscopic Transaxillary Subpectoral Breast Augmentation

University of British Columbia1 site in 1 countryMay 2013
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ConditionsBreast ImplantsSurgery, Plastic

Overview

Phase
N/A
Intervention
Not specified
Conditions
Breast Implants
Sponsor
University of British Columbia
Locations
1
Primary Endpoint
Time to return to baseline as measured on Visual Analogue Scale for pain
Status
Withdrawn
Last Updated
11 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this study is to determine whether implementing a rehabilitation program can improve the post-operative time to pain free living after breast augmentation.

Registry
clinicaltrials.gov
Start Date
May 2013
End Date
September 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •women who undergo endoscopic transaxillary subpectoral breast augmentation
  • •women above the age of 18 years
  • •women with a BMI 18-27

Exclusion Criteria

  • •women who underwent previous breast reconstruction (cosmetic or therapeutic)
  • •women who underwent previous chest surgery
  • •women with previous chest trauma
  • •women who underwent previous shoulder/arm surgery
  • •women with previous shoulder/arm injury
  • •women who smoke
  • •women who are Immunocompromised

Outcomes

Primary Outcomes

Time to return to baseline as measured on Visual Analogue Scale for pain

Time Frame: Baseline, six months, and one year after surgery

Secondary Outcomes

  • Time to return to bilateral shoulder baseline range of motion(Baseline, six months, and one year after surgery)
  • Change in psychosocial outcomes as measured by the BREAST-Q questionnaire(Baseline, six months, and one year after surgery)

Study Sites (1)

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