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Breast Augmentation Rehabilitation Program

NCT01857765 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2014-10-13

No results posted yet for this study

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

  • Breast Implants
  • Surgery, Plastic

Interventions

BEHAVIORAL

Rehabilitation

Range of motion stretching exercises

BEHAVIORAL

Follow-up

Follow-up with surgeon's clinic

Sponsors & Collaborators

  • University of British Columbia

    lead OTHER

Principal Investigators

  • Erin Brown, MD · University of British Columbia

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2014-09-30
Completion
2014-09-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01857765 on ClinicalTrials.gov