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Lack of body water in the normal population

Fluid retention in the normal population

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12215472
Enrollment
40
Registered
2016-11-18
Start date
2016-10-17
Completion date
Unknown
Last updated
2024-01-29

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

Conditions

Fluid retention Signs and Symptoms

Interventions

For the first week of the study participants are asked to continue their normal eating and drinking habits and also to record their dietary/fluid intake and provide daily urine samples. These urine sa

Sponsors

Södertälje Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Healthy hospital workers 2. Found after screening to have either concentrated urine or diluted urine

Exclusion criteria

Exclusion criteria: 1. Medical disease requiring daily medication 2. Any kind of kidney disorder

Design outcomes

Primary

MeasureTime frame
Composition of urine (urine colour, urinalysis of osmolality, specific weight, and creatinine) is assessed using urinalysis conducted on samples collected daily from baseline to the end of the second week.

Secondary

MeasureTime frame
1. Food and fluid intake throughout the study is assessed using food/fluid diaries throughout the both weeks of the study 2. Heart auscultation is assessed by a stethoscope at baseline and at 1 and 2 weeks 3. Blood pressure by Nexfin hemodynamic monitor at baseline and at 1 and 2 weeks 4. Passive leg test by Nexfin hemodynamic monitor at baseline and at 1 and 2 weeks 5. Bioimpednace for measurement of body fluid volumes at baseline and at 1 and 2 weeks

Countries

Sweden

Contacts

Public ContactRobert Hahn
robert.hahn@sll.se+46 8 55024670

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 9, 2026