WithdrawnNot Applicable

Breast Augmentation Rehabilitation Program

Stopped: The resident in charge of the project has graduated so we decided to close this study

Canada0Started 2013-05

Plain-language 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.

Who can participate

Age range18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

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

Timeframe: Baseline, six months, and one year after surgery

Trial details

NCT IDNCT01857765

SponsorUniversity of British Columbia

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2014-09

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