NCT04728178

Comparison of Perioperative Standard Fluid Management and Goal-Directed Fluid Management

Completed NA Last updated 28 January 2021

What this trial tests

NA trial testing Crystalloid solution in Perioperative Fluid Management in 60 participants. Completed in 1 May 2019.

Timeline

1 October 2017

Primary endpoint
1 January 2019

1 May 2019

Quick facts

Lead sponsor	Istanbul University
Phase	NA
Status	Completed
Study type	INTERVENTIONAL
Allocation	randomized
Design	parallel
Masking	none
Primary purpose	treatment
Enrollment	60
Start date	1 October 2017
Primary completion	1 January 2019
Estimated completion	1 May 2019
Sites	1 location across Turkey (Türkiye)

Drugs / interventions tested

• Crystalloid solution
• Colloid solution

Conditions studied

• Perioperative Fluid Management — all drugs for Perioperative Fluid Management →

Sponsor

Istanbul University

Who can join

Adults 18 to 80, any sex, with Perioperative Fluid Management. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To compare the goal-directed fluid therapy based on the data obtained from the hemodynamic monitoring system, which provides continuous CO, SV and SVV measurements through arterial pressure wave with standard fluid therapy in perioperative fluid management of patients undergoing head and neck surgery.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

1. Comparison of Stroke Volume Variation-based goal-directed Therapy Versus Standard Fluid Therapy in Patients Undergoing Head and Neck Surgery: A Randomized Controlled Study
   Turkut N, Altun D, Canbolat N, Uzuntürk C, et al · · 2022 · cited 2× · PMID 35965423 · DOI 10.4274/balkanmedj.galenos.2022.2022-1-88