A Randomized Trial of Standard of Care Sternal Precautions VS Self Managed Care

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Our study aims to compare postoperative outcomes, postoperative pain and postoperative quality of lives in patients who receive the standard sternal precautions to those in patients who received self-managed sternal precautions following sternotomy for cardiac surgeries. The purpose of the study is to see if self-managed sternal precautions following sternotomy for cardiac surgeries lead to better quality of lives while maintaining same postoperative pain and rate of postoperative adverse events than standard sternal precautions. Postoperative pain and postoperative quality of lives will be assessed by phone call surveys. Postoperative outcomes will be measured by following the patients for up to a year using electronic medical record.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Undergoing a sternotomy, English speaking, 18-70 years old, able to ambulate independently

Locations
United States
Illinois
The University of Chicago
RECRUITING
Chicago
Contact Information
Primary
Leila Yazdanbakhsh
leila.yazdanbakhsh@bsd.uchicgao.edu
773-834-5087
Backup
Carlisa Dixon
cdixon520@bsd.uchicago.edu
773-834-4337
Time Frame
Start Date: 2022-06-01
Estimated Completion Date: 2026-06
Participants
Target number of participants: 64
Treatments
Experimental: Arm 1
Arm 1 will receive instruction to use pain and discomfort as the safe limits for their upper limb use during daily activities at post operative discharge.
Active_comparator: Arm 2
Arm 2 will receive the standard sternal precautions at time of post operative discharge.
Related Therapeutic Areas
Sponsors
Leads: University of Chicago

This content was sourced from clinicaltrials.gov