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Clinical Trials/NCT02479581
NCT02479581
Completed
Phase 2

The Safety and Efficacy of the Enhanced Recovery After Surgery(ERAS) Applied on Cardiac Surgery With Cardiopulmonary Bypass: a Single Center, Randomized, Controlled Clinical Study

Xiangya Hospital of Central South University1 site in 1 country226 target enrollmentJuly 2015

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Valvular Heart Disease
Sponsor
Xiangya Hospital of Central South University
Enrollment
226
Locations
1
Primary Endpoint
The length of hospital stay
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This study evaluates the enhanced recovery after surgery (ERAS) concept over conventional postoperative care in patients with heart valve disease undergoing cardiac surgery with cardiopulmonary bypass. Half of participants will adherence to the ERAS, while the other half will under the conventional postoperative care.

Detailed Description

Enhanced recovery after surgery (ERAS) or fast-track surgery is a perioperative and postoperative care concept initiated in the early 1990s aiming to reduce the length of hospital stays following elective abdominal surgery. The success of ERAS depends highly on multidisciplinary teamwork and patient compliance. This study intends to compare the Enhanced Recovery After Surgery (ERAS) concept applied to patients with heart valve disease undergoing cardiac surgery with cardiopulmonary bypass under traditional perioperative management of patients, committed to reducing patient's physical and psychological stress by surgical trauma, achieve the purpose of fast recovery, in order to establish an effective perioperative management during cardiopulmonary bypass surgery, improve patients' satisfaction and to accelerate postoperative rehabilitation safely.

Registry
clinicaltrials.gov
Start Date
July 2015
End Date
May 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Xiangya Hospital of Central South University
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Heart function grade II - III (Using the cardiac function classification method formulated by American Heart Disease Institute)
  • The in - hospital was treated with extracorporeal circulation operation and general anesthesia.
  • Had a good cognition, and signed the informed consent.
  • Aged between 18 and
  • The age, clinical examination and other generally situation of the two groups of patients had no statistical significance.

Exclusion Criteria

  • Combined with other blood coagulation dysfunction, serious brain, liver and kidney dysfunction, endocrine system diseases and serious infectious disease.
  • Patients with severe mental disorders cannot cooperate with the treatment.
  • Emergency operation
  • Have taboo of Echocardiography and pulmonary catheterization by echocardiography.
  • Patients have been fitted with a pacemaker.
  • Allergic to erythropoietin.
  • Suspected or had alcohol, drug abuse history.
  • Spinal deformity or paravertebral lesions.

Outcomes

Primary Outcomes

The length of hospital stay

Time Frame: From pre-surgery to discharge, up to 8 weeks

The postoperative hospital time

Time Frame: From pre-surgery to discharge, up to 4 weeks

The time of readiness to discharge

Time Frame: From pre-surgery to discharge, up to 4 weeks

Length of ICU stay

Time Frame: From entering the ICU to roll out, up to 4 weeks

Hospitalization cost

Time Frame: When the patient is discharged

Secondary Outcomes

  • C-reactive protein(baseline and 5 days after operation)
  • Serum Creatinine(baseline and 5 days after operation)
  • Postoperative tracheal tube time(From the end of surgery to the removal of tracheal tube, up to 4 weeks)
  • Time to first bowel movement(From the end of surgery to first exhaust, up to 2 weeks)
  • Hemoglobin(baseline and 5 days after operation)
  • Troponin I(baseline and 5 days after operation)
  • Perioperative major adverse events(From pre-surgery to discharge, up to 4 weeks)
  • Procalcitonin(baseline and 5 days after operation)
  • Duration of mechanical ventilation after surgery(From the end of surgery to the recovery of spontaneous breathing, up to 4 weeks)
  • Postoperative time to first exhaust(From the end of surgery to first exhaust, up to 2 weeks)
  • Erythrocyte Sedimentation Rate(baseline and 5 days after operation)
  • Vasoactive drugs Support Hours(From the start of drugs to stop them, up to 4 weeks)
  • N-terminal B-type natriuretic peptide(NT-proBNP)(baseline and 5 days after operation)

Study Sites (1)

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