Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01857765

Breast Augmentation Rehabilitation Program

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

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
University of British Columbia · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALRehabilitationRange of motion stretching exercises
BEHAVIORALFollow-upFollow-up with surgeon's clinic

Timeline

Start date
2013-05-01
Primary completion
2014-09-01
Completion
2014-09-01
First posted
2013-05-20
Last updated
2014-10-13

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01857765. Inclusion in this directory is not an endorsement.

Breast Augmentation Rehabilitation Program (NCT01857765) · Clinical Trials Directory