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The Benefits of the Use of a Support Bra in Women Undergoing Coronary Artery By-Pass Graft Surgery

NCT02864186 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 190

Last updated 2021-03-02

No results posted yet for this study

Summary

That study have the primary purpose identify if exist difference to the healing and quality of life between women that use of a surgical support bra, common support bra and without support bra after coronary artery bypass graft surgery.

To do this, will be assessed pain, healing of the wound (dehiscence, infection) and quality of life life through specific instruments.

Conditions

  • Quality of Life
  • Wound Complications
  • Pain

Interventions

DEVICE

control

Women wont use support bra 24 hours a days for six months

DEVICE

surgical support bra

Women will use surgical support bra 24 hours a day for six months

DEVICE

common support bra

Women will use common support bra 24 hours a day for six months

Sponsors & Collaborators

  • University of Sao Paulo

    lead OTHER

Principal Investigators

  • LUIZ AM CESAR, MD, PhD · INSTITUTO DO CORAÇÃO, HOSPITAL DAS CLÍNICAS DA FACULDADE DE MEDICINA DA UNIVERSIDADE DE SÃO PAULO

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-01-26
Primary Completion
2018-08-30
Completion
2018-08-30

Countries

  • Brazil

Study Locations

More Related Trials

Entities

Diseases

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 NCT02864186 on ClinicalTrials.gov