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ERAS in Colorectal Surgery: Benefits of Late Adoption

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University Hospital Basel

Status

Completed

Conditions

Colorectal Disorders
Colorectal Neoplasms
Colorectal Cancer

Treatments

Procedure: ERAS protocol

Study type

Observational

Funder types

Other

Identifiers

NCT05773248
2023-00221

Details and patient eligibility

About

The aim of this single-center retrospective cohort study is to explore the effect of late adaptation of an ERAS protocol in a high-volume colorectal surgical unit.

The primary endpoint is the surgical outcome measured by early postoperative complications, defined by the comprehensive complications index. Secondary endpoints include amongst others LOS (length of stay), cost analysis, short-term follow-up in the ERAS group.

Full description

At Clarunis - University Center for Gastrointestinal and Liver Diseases at St. Claraspital between 2019 und 2020, all colorectal patients were treated according to a standardized perioperative protocol. As of 2021 until today, an ERAS protocol was established and all colorectal patients who met inclusion criteria participated in this program automatically as part of a new standardized care. Perioperative data was collected in a clinical information system (Phoenix - CGM Clinica Information Systeml).

In this retrospective cohort study, we compare demographic, perioperative and postoperative data among the two groups "ERAS" and "non-ERAS" using a weighted propensity score analysis for patients who underwent surgery as part of the ERAS program and for patients without a standardized ERAS protocol.

All patients treated at the colorectal unit from 2019 until August 2022 and who are considered for the analysis have given written general consent for the use of health-related data for research projects (attached to this document).

Enrollment

456 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • written general informed consent
  • patients undergoing a colorectal procedure between 2019 and August 2022 at colorectal unit, Santa Clara Hospital, Basel

Exclusion criteria

  • All patients undergoing an emergency procedure or a combined procedure with the colorectal procedure not being the main indication for surgical treatment (i.e. gynecological debulking, liver resection, etc.) were excluded from the analysis.

Trial design

456 participants in 2 patient groups

Standard care
ERAS
Treatment:
Procedure: ERAS protocol

Trial contacts and locations

1

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Central trial contact

Julian Süsstrunk, Dr.; Daniel Steinemann, PD Dr.

Data sourced from clinicaltrials.gov

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