UnknownN/AOther

Enhanced Recovery After Surgery (ERAS) in Coronary Artery Bypass Graft / Off Pump Coronary Artery Bypass (CABG/OPCAB)

Sponsored by Silesian University of Medicine

NCT ID
NCT03956420
Target Enrollment
100 participants
Start Date
2019-05-03
Est. Completion
2021-05

About This Study

It has been assumed that some elements of the ERAS protocol may contribute to the reduction of complications and improve the satisfaction of patients undergoing coronary artery bypass surgery. Elements of the ERAS strategy will be tested in this study. The elements that prove to be feasible and have a positive effect on the treatment process will be introduced into everyday clinical practice. In the next stage of the research, we are planning to investigate whether the introduction of the ERAS strategy has had a long-term positive effect on the quality of life after treatment (a survey 1 month and 6 months after leaving the hospital).

Conditions Studied

Coronary Artery DiseaseCoronary Stenosis

Interventions

  • Premedication visit
  • Preoperative period
  • Preoperative period
  • Postoperative period
  • Intraoperative period
  • Intraoperative period
  • Intraoperative period
  • Intraoperative period
  • Intraoperative period
  • Intraoperative period

Eligibility

Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* CABG/OPCAB (Coronary Artery Bypass Surgery/Off Pump Coronary Bypass Surgery).
* Left ventricular ejection fraction above 35% (EF ≥ 35%).
* The operation was performed in a planned mode.

Exclusion Criteria:

* Haematological diseases and the associated increased risk of bleeding in the early postoperative period. Patients taking anticoagulants until the day of surgery with the exception of aspirin.
* Neurological disorders, stroke with persistent symptoms, dementia.
* Chronic lung disease with hypoxia and the need for regular medication.
* Inability to move independently, disability preventing efficient rehabilitation, prolonged use of painkillers.
* Emergency surgery, reoperation.
* Return to the operating room regardless of the reason (resternotomy).
* Perioperative infarction with circulatory destabilization.

Study Locations (1)

Upper-Silesian Medical Centre of the Silesian Medical University
Katowice, Polska, Poland

This trial is not recruiting

This study is currently not accepting new participants.

Find recruiting trials
Data Source
ClinicalTrials.gov

Last updated from source