Status:

COMPLETED

Assessment of Circulating Copeptin Levels in Healthy Subjects and Patients With Renal Insufficiency After Oral Water Load and Hypertonic Saline Infusion

Lead Sponsor:

Hospital Centre Biel/Bienne

Collaborating Sponsors:

Brahms AG

Conditions:

Hypoosmolality

Hyperosmolality

Eligibility:

All Genders

18-80 years

Brief Summary

The are 2 principal goals in this study: 1. To measure plasma copeptin levels in healthy subjects and to correlate them with plasma AVP concentrations and urine osmolalities in iso-, hypo-, and hyper...

Eligibility Criteria

Inclusion

  • chronic renal failure grade I through IV
  • healthy age-matched controls

Exclusion

  • chronic renal failure grade V
  • heart failure
  • liver disease
  • nephrotic syndrome
  • anemia (hemoglobin level \< 100 g/L)
  • uncontrolled hypertension (systolic BP \> 160 mmHg; diastolic BP \> 95 mm Hg)
  • coexisting severe disease
  • known thyroid disease
  • known hypocortisolism
  • known hypercortisolism
  • known diabetes insipidus
  • pregnancy
  • lactation

Key Trial Info

Start Date :

July 1 2008

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

October 1 2009

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT00696605

Start Date

July 1 2008

End Date

October 1 2009

Last Update

February 27 2017

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Clinic of Internal Medicine, Hospital Center

Biel/Bienne, Switzerland, 2501

Assessment of Circulating Copeptin Levels in Healthy Subjects and Patients With Renal Insufficiency After Oral Water Load and Hypertonic Saline Infusion | DecenTrialz