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Breast Augmentation Rehabilitation Program

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

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01857765
Enrollment
0
Registered
2013-05-20
Start date
2013-05-31
Completion date
2014-09-30
Last updated
2014-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Implants, Surgery, Plastic

Keywords

rehabilitation, reconstructive surgery

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.

Interventions

BEHAVIORALRehabilitation

Range of motion stretching exercises

BEHAVIORALFollow-up

Follow-up with surgeon's clinic

Sponsors

University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
Time to return to baseline as measured on Visual Analogue Scale for painBaseline, six months, and one year after surgery

Secondary

MeasureTime frame
Time to return to bilateral shoulder baseline range of motionBaseline, six months, and one year after surgery
Change in psychosocial outcomes as measured by the BREAST-Q questionnaireBaseline, six months, and one year after surgery

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026