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Fluid Optimisation in Laparoscopic Colorectal Procedures

U

University Medical Centre Ljubljana

Status

Completed

Conditions

Perioperative Complication

Treatments

Procedure: Perioperative fluid optimisation

Study type

Interventional

Funder types

Other

Identifiers

NCT04719884
127/5/12

Details and patient eligibility

About

Goal-directed fluid therapy (GDFT) with hemodynamic monitoring may not be of benefit to all elective patients undergoing major abdominal surgery, particularly those managed in Enhanced Recovery After Surgery protocols (ERAS) setting.

Full description

Our study compared two groups of patients undergoing elective laparoscopic colorectal surgery: a control group (CG) in which standard haemodynamic monitoring was used, and a study group (SG) in which extended haemodynamic monitoring was applied with appropriate intraoperative interventions. Differences in intraoperative fluid management, hospital stay, and postoperative morbidity were observed.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients, undergoing elective laparoscopic colorectal surgery

Exclusion criteria

  • Patients with cardiac arrhythmias

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Control group
No Intervention group
Description:
Standard perioperative anesthesia management
Study group
Active Comparator group
Description:
Perioperative extended haemodynamic monitoring of fluid loading, cardiac output and changes of peripheral vascular resistance by analysing the arterial curve was provided by non-invasive haemodynamic monitoring (LIDCO Rapid, Lidco Ltd., United Kingdom).In SG fluid optimisation was performed before pneumoperitoneum and after abdominal desuflation with actions to achieved CI, MAP and SI within 80% of baseline values.
Treatment:
Procedure: Perioperative fluid optimisation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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