Goal Directed Fluid Therapy Using Cardiometry Monitor in Patients Undergoing Major Spine Surgery in The Prone Position

Goal Directed Fluid Therapy Based on Stroke Volume Variation and Oxygen Delivery Index in Patients Undergoing Major Spine Surgery in the Prone Position

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

PACTR

Registry ID

PACTR202007901764021

Enrollment

Registered

2020-07-17

Start date

2020-06-01

Completion date

Unknown

Last updated

2026-01-27

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

Conditions

Circulatory System Surgery Orthopaedics Anaesthesia

Interventions

Liberal fluid therapy

Goal directed fluid therapy

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. American Society of Anesthesiologist (ASA) status I-II. 2. Posterior spine arthrodesis involving at least 5 vertebral instrumentational levels. 3. Age between 15 and 65 years. 4. A planned postoperative intensive care unit admission

Exclusion criteria

Exclusion criteria: 1. Patients with known heart disease or any cardiac arrhythmia. 2. Patients with any abnormality in baseline coagulation test, creatinine or liver enzymes. 3. Patients with vascular lesions

Design outcomes

Primary

Measure	Time frame
to evaluate whether a Goal Directed Fluid Therapy (GDFT) protocol will be effective in reducing perioperative red blood cells transfusions.	—

Secondary

Measure	Time frame
to compare the effects of Goal Directed Fluid Therapy with conventional fluid therapy as regards total amount of fluids transfused, perioperative complications and postoperative length of ICU stay.	—

Countries

Egypt

Contacts

Public ContactAhmed Abdo

Professor of anaesthesia and surgical intensive care

smsmsmsm10090@gmail.com+201119277287

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Feb 16, 2026