Breast Augmentation Rehabilitation Program

Breast Implants Clinical Trial

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

Status Withdrawn

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01857765
Study type	Interventional
Source	University of British Columbia
Contact
Status	Withdrawn
Phase	N/A
Start date	May 2013
Completion date	September 2014

View Details

See also
Status	Clinical Trial	Phase
Not yet recruiting	`NCT06013514` - Post-market Prospective Clinical Study of Nagor Perle Mammary Implants
Recruiting	`NCT02777476` - Clinical Performance of B-Lite® Light Weight Breast Implant	N/A
Recruiting	`NCT06147661` - Primary Aesthetic Breast Augmentation: Comparative Study Between Breast Implants and Autograft of Adipose Tissue
Completed	`NCT00858052` - Core Study of the Safety and Effectiveness of IDEAL IMPLANT(R) Saline-filled Breast Implants	N/A
Completed	`NCT01874652` - Assessment of Safety & Efficacy of Light Weight Breast Implant	Phase 2
Active, not recruiting	`NCT03579901` - Study of the Safety and Effectiveness of Motiva Implants®	N/A