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NCT Number: NCT06034990

ICU Fluid Utilization Survey in Southeast Asia

The objective of this study is to examine the use of different types of fluids for resuscitation in different phases of fluid management in 3 types of critically ill patients including (1) not bleeding, not septic but need volume resuscitation (representing normal condition), (2) bleeding but not septic (representing normal vascular integrity but with a loss of intravascular colloids), (3) septic (representing the condition with increase vascular permeability and endothelium damage) in the ICU within Southeast Asia.

The data are collected by a 10-min online survey administered to included physicians which will be distributed via multiple online channels through representatives of each countries.

Recruiting

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Chulalongkorn university

Bangkok, 10330, Thailand

Location status: Recruiting

Location contact

Nattachai Srisawat, MD

CONTACT

[email protected]

6622564000 ext. 3597

About this study

The objective of this study is to examine the use of different types of fluids for resuscitation in different phases of fluid management in 3 types of critically ill patients including (1) not bleeding, not septic but need volume resuscitation (representing normal condition), (2) bleeding but not septic (representing normal vascular integrity but with a loss of intravascular colloids), (3) septic (representing the condition with increase vascular permeability and endothelium damage) in the ICU within Southeast Asia, and to determine whether co-morbidities with hypoalbuminemia, clinician specialties, hospital practice settings, geographic locations and re-imbursement limitation especially for colloids influence the practice patterns of fluid utilization in different phases in the 3 types of patients. Ultimately, the information provided by this study could also provide basic background information for the design of future clinical trials regarding fluid resuscitation strategies.

The data are collected by a 10-min online survey administered to included physicians which will be distributed via multiple online channels through representatives of each countries.

The survey will start with an inform-consent form prior to starting the survey questions which consist of 13-item questionnaire obtaining information on

  • Demographics data of clinicians taking the survey on primary specialty, region or country of practice and hospital settings.
  • Preferences for volume status indicators.
  • Preferences for fluid resuscitation in 3 types of patients (1. Septic 2. bleeding but not septic 3. not bleeding and not septic) during resuscitation and optimization phase.
  • Preferences for fluid resuscitation in the 3 types of patients with hypoalbuminemia including (1) cirrhosis (2) nephrotic syndrome (3) other significant hypoalbuminemia during resuscitation/optimization phase and stabilization phase
  • The reasons for using colloids for volume expansion
  • The experience of adverse reactions to albumin
  • The awareness and importance of non-oncotic properties of albumin
  • The impact of reimbursement for colloids on resuscitation fluid choice

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Specialty must be in Anesthesiology, Surgery, Critical Care Medicine, Pulmonology, Nephrology, Internal Medicine, General Practitioner
  • Practice must be in Southeast Asia hospitals
  • Must work in Surgical ICU, Medical ICU , and/or Mixed ICU

Exclusion criteria

1.Physicians who worked in cardiac, neurology or pediatric ICUs

Treatment and study plan

10-min online survey

Other

This is a cross-sectional study. The data are collected by a 10-min online survey administered to included physicians which will be distributed via online channels such as such as official website or Facebook pages of Society of intensive care or Society of nephrology of corresponding countries.

Primary outcomes

  1. Fluid resuscitation practice pattern

    Time frame: 1/9/23-1/9/24

    Preferences for fluid resuscitation in 3 types of patients (1. Septic 2. bleeding but not septic 3. not bleeding and not septic) during resuscitation and optimization phase.

Secondary outcomes

  1. Preferences for volume status indicators.

    Time frame: 1/9/23-1/9/24

    Preferences for volume status indicators and diagnostic tools

  2. Fluid resuscitation practice pattern in hypoalbuminemic state

    Time frame: 1/9/23-1/9/24

    Preferences for fluid resuscitation in the 3 types of patients with hypoalbuminemia including (1) cirrhosis (2) nephrotic syndrome (3) other significant hypoalbuminemia during resuscitation/optimization phase and stabilization phase

Study contacts

Contact information is provided by the study sponsor or research team.

Nattapakorn Mai-on, MD

CONTACT

[email protected]

+66970051116

Sponsors and collaborators

Lead sponsor

Chulalongkorn University

Other

Registry information

Acronym: Fluid-SEA

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Sep 13, 2023
Registry last updated
Aug 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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