Enhanced Recovery After Surgery in patients with colorectal, liver, pancreatic, thoracic, upper gastrointestinal tract, and bariatric surgery – ERAS
Not Applicable
Recruiting
- Conditions
- Colon, liver, pancreatic, thoracic, upper gastrointestinal tract, and bariatric surgeries.
- Registration Number
- DRKS00030908
- Lead Sponsor
- Chirurgische Klinik, Campus Charité Mitte und Campus Virchow-Klinikum, Charité - Universitätsmedizin Berlin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 500
Inclusion Criteria
Written informed consent to participate in the study after being educated on the study by a physician.
- Patients with planned elective surgery
Exclusion Criteria
- Lack of written informed consent to participate in the study
- Patients who had to undergo emergency surgery at short notice instead of the planned elective surgery
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Complication rates (Clavien-Dindo I-V, general complication rates, surgical complication rates), length of stay.
- Secondary Outcome Measures
Name Time Method Adherence to ERAS measures, recovery after organ resection surgery measured by postoperative mobilization time per day, time to first stool, time to oralization of drug therapy, and time to regain preoperative mobility.<br>Costs, revenues, profits of treatment.