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Clinical Trial NCT05538351 for Acute Kidney Injury is active, not recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here. | ||
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A Study to Support the Development of the Enhanced Fluid Assessment Tool for Patients With Acute Kidney Injury
Clinical Trial NCT05538351 is an observational study for Acute Kidney Injury that is active, not recruiting. It started on September 9, 2022 with plans to enroll 120 participants. Led by University of Hertfordshire, it is expected to complete by August 1, 2026. The latest data from ClinicalTrials.gov was last updated on December 5, 2025.
Brief Summary
Acute Kidney Injury (AKI) is the sudden and recent reduction in kidney function. This can be detected by measuring a rise in blood creatinine level or from a reduction in urine. Reasons for developing AKI, include dehydration, low blood pressure, medication and infection. When the kidneys stop working, there can be a build-up of toxins and fluid. It is extremely important to identify a patient's fluid status as too little can cause further damage to the kidneys and too much can be harmful. Assessment is varied and often inaccurate and there needs to be a standard approach to fluid assessment.
Detailed Description
Acute Kidney Injury (AKI) is the sudden and recent reduction in kidney function. This can be detected by measuring a rise in blood creatinine level or from a reduction in urine. Reasons for developing AKI, include dehydration, low blood pressure, medication and infection. When the kidneys stop working, there can be a build-up of toxins and fluid. It is extremely important to identify a patient's fluid status as too little can cause further damage to the kidneys and too much can be harmful. Assessment is varied and often inaccurate and there needs to be a standard approach to fluid assessment.
Aim:
To develop an Enhanced Fluid Assessment Tool for patients with AKI.
Workstream 1:
Aim: To identify what methods are useful to assess fluid in a patient with AKI. The fluid assessment techniques that are useful and are used, bioimpedance and patient reported signs and symptoms.
Workstream 2:
Aim: To identify the best methods of determining fluid status in a patient with AKI The findings from Workstream 1 will be used to rank the most useful fluid assessment techniques. This will lead to the development of the enhanced fluid assessment tool.
Workstream 3:
Aim: To assess if the tool is practical and clinically useful in determining a patient's fluid status.
The terminology and language will be reviewed and the tool will be used to assess patients and to determine the patients fluid status.
Official Title
A Study to Support the Development of the Enhanced Fluid Assessment Tool for Patients With Acute Kidney Injury
Conditions
Acute Kidney InjuryOther Study IDs
- HSK/PGR/NHS/02973
NCT ID Number
Start Date (Actual)
2022-09-09
Last Update Posted
2025-12-05
Completion Date (Estimated)
2026-08-01
Enrollment (Estimated)
120
Study Type
Observational
Status
Active, not recruiting
Keywords
dehydration
hypotension
Acute Kidney Injury
hypovolaemia
respiratory rate
extracellular fluid
hypertension
body weight changes
pulmonary oedema
oedema
signs and symptoms
blood volume
hypotension
Acute Kidney Injury
hypovolaemia
respiratory rate
extracellular fluid
hypertension
body weight changes
pulmonary oedema
oedema
signs and symptoms
blood volume
Arms / Interventions
| Participant Group/Arm | Intervention/Treatment |
|---|---|
Fluid assessment All patients enrolled in this study will have a clinical assessment to identify hydration status, patient reported signs and symptoms of hydration and Bioimpedance using the Body composition Monitor (BCM). | Body Composition Monitor (BCM) The hydration status of each participant from the clinical assessment and the patient reported signs and symptoms will be compared with the readings from bioimpedance (BCM machine). |
Primary Outcome Measures
Secondary Outcome Measures
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
To identify the components of clinical assessment deemed useful in determining fluid status in patients with AKI. | Identifying the components of a volume assessment as defined in RCP (2015) Acute care toolkit and a scoping review on fluid assessment. Assessment includes; physiological parameters including blood pressure, weight changes, and physical examination, including identifying any signs of oedema or dehydration and history taking. | Within 72 hours of admission |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
To identify fluid status of patients with AKI using multiple assessments, including Bioimpedance, objective and subjective clinical assessments. | Bioimpedance measures fluid status and location of this fluid within the body. | Within 72 hours of admission |
To identify patient-focussed signs and symptoms of hydration in AKI | The patient with acute kidney injury will be asked to describe their signs and symptoms relating to acute kidney injury. | Within 72 hours of admission |
To evaluate whether fluid status of patients is related to: Stage of AKI, Cause of AKI, Length of stay, NEWS2 Measurements | To identify descriptive data from the patients medical notes. | At 30 days after admission |
To evaluate whether fluid status of patients is related to: Physical assessment (JVP, oedema, skin, respiratory, lying and standing BP, passive leg raise), Blood results: urea and creatinine, electrolytes, albumin, haemoglobin and bicarbonate. | Comparison between patients in different fluid status groups will be compared using t-tests (or non-parametric comparisons), or Chi squared (χ2) tests. Multi variable models will be explored to evaluate the relationship of measured variables to fluid status using logistic models. | Within 72 hours of admission |
To evaluate whether fluid status is related to: Fluid balance chart/ trends and documentation (positive or negative balance) , Weight trends, Charlson Co-morbidity index | A multivariate analysis of clinical characteristics (specifically as listed in the primary objective) to investigate their predictive effect for mortality at 30 days. Variables that are significant in univariate models at the 10% level will be then included in a multivariable regression analysis. | At 30 days since admission |
To evaluate whether fluid status is related to: Outcome: Renal Replacement therapy (RRT) during admission/ Recovery of kidney / dialysis dependence at 30 days/ Intensive care admission • Mortality (hospital 30-days) • Readmission (within 30 days) | A multivariate analysis of clinical characteristics (specifically as listed in the primary objective) to investigate their predictive effect for mortality at 30 days. Variables that are significant in univariate models at the 10% level will be then included in a multivariable regression analysis. | At 30 days after admission |
Eligibility Criteria
Eligible Ages
Adult, Older Adult
Minimum Age
18 Years
Eligible Sexes
All
- Workstream 1 and 3 (phase 3):
Patients who will be included in the study will be Adult patients (over 18 years old) identified as having an acute kidney injury (AKI) within 72 hours of admission to hospital.
Workstream 2:
Experts in fluid assessment (Doctors, Nurses and AHPs). Persons included will be experts in their field of practice and have a recognised expertise in fluid assessment.
Workstream 3:
Phase 1: Experts in fluid assessment (Doctors, Nurses and AHPs). Phase 2: Staff nurses currently working on a clinical ward.
- Patients who have kidney failure requiring dialysis or who are being conservatively managed.
- Patients who are receiving end of Life (EoL) care.
- Patients who have a pacemaker as this interferes with bioimpedance (WS1+3).
- There is no baseline creatinine.
- The patient has acquired an AKI 72 hours after admission to hospital.
- The patient has acute coronary syndrome
University of HertfordshireEast and North Hertfordshire NHS TrustNo contact data.
1 Study Locations in 1 Countries
East and North Hertfordshire NHS Trust, Lister Hospital, Stevenage, United Kingdom