PreRELIEF - The haemodynamic consequence of restriction compared to liberal intravenous fluid therapy in patients undergoing major abdominal surgery.
Not Applicable
Completed
- Conditions
- Major Abdominal SurgeryFluid therapy intraoperativeHaemodynamics, specifically stroke volume and preload responsivenessAnaesthesiology - Other anaesthesiologyCardiovascular - Normal development and function of the cardiovascular system
- Registration Number
- ACTRN12615000125527
- Lead Sponsor
- Dr Tuong Dien Phan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Patients must already be recruited the RELIEF trial (ClinicalTrials.gov Identifier: NCT01424150) which is currently recruiting.
Incusions criteria include adults over 18 years of age and
all types of open or laprascopic assisted abdominal or pelvic surgery with a duration of atleast 2 hours and an expected hospital stay of at least 3 days.
Exclusion Criteria
Urgent surgery
ASA 5
Chronic renal failure requiring dialysis
Pulmonary or Cardiac Surgery
Liver Ressection
Minor/Intermediate Surgery
in addition
Patients who may have an inappropriate response to PLR.
Patients with a contraindication to a PLR
Patients in whom an ODM cannot be placed
Patients in whom the primary anaesthetist chooses to use GDT
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method