Fluid Responsiveness Tests in Critically Ill Patients During Admission to the Intensive Care Unit

NCT06729268 | Completed

• 1 other identifier: PossFluRespTests
• Study Type: observational
• Target: 389
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this observational study is to investigate the prevalence of conditions allowing the performance fluid responsiveness tests in critically ill patients during admission to the intensive care unit.

Conditions

Shock Circulatory; Heart Failure; Hypovolemia

Outcome Measures

Primary Outcomes (1)

• To assess the prevalence of conditions allowing the performance fluid responsiveness tests during admission to the intensive care unit.

  The primary aim of the study is to assess the prevalence of conditions allowing the performance fluid responsiveness tests during admission to the intensive care unit.

  Six hours after admission to the intensive care unit

Secondary Outcomes (2)

• To assess which fluid responsiveness test based on heart-lung interactions can be applied most often during admission to the intensive care unit

  Six hours after admission to the intensive care unit

• To assess the percentage of patients in shock whom fluid responsiveness tests can be performed during admission to the intensive care unit

  Six hours from the admission to the intensive care unit.

Study Arms (1)

Patients treated in the intensive care unit

Patients treated in the intensive care unit during the first six hours after admission.

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

Adult patients admitted to the intensive care unit

You may qualify if:

• \. Adult patients admitted to the intensive care unit

You may not qualify if:

• Age under 18
• The researcher unavailable in the intensive care unit
• Patient assessment cannot be completed within the first six hours after admission to the ICU

Sponsors & Collaborators

• Uniwersytecki Szpital Kliniczny w Opolu: lead

Study Sites (1)

Department of Anesthesiology and Intensive Care, Uniwersytecki Szpital Kliniczny w Opolu

Opole, Opole Voivodeship, 45-401, Poland

Location

MeSH Terms

Conditions

Shock; Heart Failure; Hypovolemia

Condition Hierarchy (Ancestors)

Pathologic Processes; Pathological Conditions, Signs and Symptoms; Heart Diseases; Cardiovascular Diseases

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: December 7, 2024
• First Posted: December 11, 2024
• Study Start: April 3, 2023
• Primary Completion: May 27, 2024
• Study Completion: May 27, 2024
• Last Updated: December 31, 2024

Record last verified: 2024-11

Data Sharing

• IPD Sharing: Will not share

Locations

PL (1)