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Hydration following acute stroke

An investigation into the hydration status of acute stroke patients receiving thickened versus thin fluids

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12607000533493
Enrollment
30
Registered
2007-10-17
Start date
2007-07-16
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

This 7 week cross sectional study aims to get a 'snap shot' of the hydration status of stroke patients admitted to Flinders Medical Centre and the determine any significant differences in the hydration status and fluid intake between those receiving thickened fluids compared with stroke patients on thin fluids. This project also seeks to determine whether there are any associations between hydration status and rehabilitation outcomes post acute stroke. This will provide data to ascertain whether dehydration is a common phenomenon among acute stroke patients admitted to flinders medical centre and whether urine specific gravity is used in clinical practice to determine if stroke patients are dehydrated, and therefore, require additional fluid subcutaneously or intravenously to ensure adequate hydration.

Interventions

This is a cross sectional study of acute stroke patients in which fluid intake will be recorded over a 24 hour period and hydration status will be assessed by measuring the urine specific gravity (USG) of a collected urine sample. Routine blood tests will also be accessed to determine biochemical indices of hydration. All tests will be performed over a 48 hour period for each patients.

Sponsors

Nutrition & Dietetics Department, Flinders Medical Centre
Lead SponsorHospital

Eligibility

Sex/Gender
All
Age
50 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

Patients admitted to Flinders Medical Centre with clinical diagnosis of a stroke of all types (ischaemic/haemorrhagic). Patient or carer able to provide informed consent.

Exclusion criteria

Patients who have had a transient ischaemic attack (TIA), are nil by mouth, or have chronic renal impairment.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026