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Completed

NCT Number: NCT03574688

The Hydration to Optimize Metabolism (H2O Metabolism) Pilot Study

This study evaluates increased hydration (1.5 L of water daily during 6 weeks) on top of habitual water intake in the lowering of the vasopressin marker copeptin and in the lowering of plasma glucose concentration in adults with signs of low water intake at recruitment (elevated levels of copeptin, high urine osmolality, low urine volume).

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Key information

Age range

20 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

KFE, Skåne University Hospital in Malmö

Malmö, 20502, Sweden

About this study

High plasma concentration of vasopressin (i.e. antidiuretic hormone) is a novel and independent risk factor for type 2 diabetes, the metabolic syndrome, cardiovascular disease and premature death. The main physiological role of vasopressin is to maintain constant plasma osmolality. Previous studies in rats and a Mendelian randomization study in humans suggest causality between elevated vasopressin concentration and elevated plasma glucose concentration. As vasopressin can be suppressed by increasing water intake, the investigators hypothesize that water supplementation in individuals with high vasopressin can lower plasma glucose and prevent diabetes.

The aim of this pilot study is to test if six weeks of water supplementation of 1.5 Liters of extra water per day in low-drinkers with high copeptin can significantly alter hydration markers in general and reduce plasma copeptin in particular. Furthermore, the investigators also aim at investigating whether this 6-week water intervention can significantly reduce fasting plasma glucose concentration.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Provision of informed consent
  • Age 20-75 years
  • High plasma concentration of copeptin of >6.1 pmol/L in women and > 10.7 pmol/L in men
  • 24-hour urine osmolality > 600 milliosmol (mosm) /kg water.

Exclusion criteria

  • 24-hour urine volume >1.5 L
  • Pregnancy or breastfeeding
  • Plasma sodium <135 mmol/L
  • Use of diuretics, lithium or SSRI drugs
  • Chronic kidney disease (estimated glomerular filtration rate < 30mL/min)
  • Heart failure
  • Inflammatory bowel disease
  • Type 1 diabetes or type 2 diabetes treated with insulin
  • Vulnerable subjects (subjects with legal guardian, with loss of personal liberty)

Treatment and study plan

Water

Dietary Supplement

Increased daily water intake with 1.5 Liters of water per day on top of habitual water intake.

Primary outcomes

  1. Fasting plasma copeptin concentration (pmol/L)

    Time frame: 6 weeks

    Change of fasting plasma copeptin between baseline and after 6 weeks of increased water intake.

Secondary outcomes

  1. 24 hour urine osmolality (mosm/kg H2O)

    Time frame: 6 weeks

    Change of 24 hour urine osmolality between baseline and after 6 weeks of increased water intake.

  2. 24 hour urine volume (L/24h)

    Time frame: 6 weeks

    Change of 24 hour urine volume between baseline and after 6 weeks of increased water intake.

  3. Drinking water (L/day)

    Time frame: 6 weeks

    Change of intake of tap and bottled water between baseline and after 6 weeks of increased water intake.

  4. Total water (L/day)

    Time frame: 6 weeks

    Change of total water intake between baseline and after 6 weeks of increased water intake.

  5. Fasting plasma glucose concentration (mmol/L)

    Time frame: 6 weeks

    Change of Fasting plasma glucose concentration between baseline and after 6 weeks of increased water intake.

Sponsors and collaborators

Lead sponsor

Region Skane

Other

Collaborators

  • Danone Global Research & Innovation Center
  • Lund University

Registry information

Acronym: H2OMetaboPilot

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Jul 2, 2018
Registry last updated
Jul 3, 2018

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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