Breast Augmentation Rehabilitation Program

University of British Columbia

Status: Withdrawn

Conditions: Surgery, Plastic; Breast Implants

Treatments: Behavioral: Follow-up; Behavioral: Rehabilitation

Study type: Interventional

Funder types: Other

Identifiers

NCT01857765

H11-02077

Details and patient eligibility

About

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.

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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0 participants in 2 patient groups

Standard of Care

Active Comparator group

Treatment:

Behavioral: Follow-up

Rehabilitation

Experimental group

Treatment:

Behavioral: Rehabilitation

Behavioral: Follow-up