Breast Augmentation Rehabilitation Program
Not Applicable
Withdrawn
- Conditions
- Breast ImplantsSurgery, Plastic
- Interventions
- Behavioral: RehabilitationBehavioral: Follow-up
- Registration Number
- NCT01857765
- Lead Sponsor
- University of British Columbia
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
- women who undergo endoscopic transaxillary subpectoral breast augmentation
- women above the age of 18 years
- women with a BMI 18-27
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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
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Rehabilitation Follow-up - Standard of Care Follow-up - Rehabilitation Rehabilitation -
- Primary Outcome Measures
Name Time Method Time to return to baseline as measured on Visual Analogue Scale for pain Baseline, six months, and one year after surgery
- Secondary Outcome Measures
Name Time Method 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
Trial Locations
- Locations (1)
University of British Columbia
🇨🇦Vancouver, British Columbia, Canada