Enhanced Recovery After Surgery in patients with colorectal, liver, pancreatic, thoracic, upper gastrointestinal tract, and bariatric surgery – ERAS

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00030908

Enrollment

500

Registered

2022-12-13

Start date

2018-07-01

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colon, liver, pancreatic, thoracic, upper gastrointestinal tract, and bariatric surgeries.

Interventions

Group 1: Patients who undergo organ resection surgery and are treated perioperatively according to the current in-house standard operating procedures of the Department of Surgery, Campus Charité Mitte

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
Complication rates (Clavien-Dindo I-V, general complication rates, surgical complication rates), length of stay.	—

Secondary

Measure	Time frame
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. Costs, revenues, profits of treatment.	—

Countries

Germany

Contacts

Public ContactJens Neudecker

Chirurgische Klinik, Campus Charité Mitte und Campus Virchow-Klinikum, Charité - Universitätsmedizin Berlin

jens.neudecker@charite.de+49 30 450 652 013

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026