Status:

COMPLETED

The Kidneys Ability to Concentrate and Dilute Urine in Patients With Autosomal Dominant Polycystic Kidney Disease

Lead Sponsor:

Regional Hospital Holstebro

Conditions:

Polycystic Kidney, Autosomal Dominant

Chronic Kidney Diseases

Eligibility:

All Genders

Phase:

NA

Brief Summary

The ability to concentrate and dilute urine is primarily regulated via vasopressin (AVP) dependent Aquaporin-2 water channels (AQP2 channels) in the kidney's collecting duct. Autosomal dominant polycy...

Detailed Description

The aim is to measure the difference in renal function, including kidney tubular function, blood pressure and vasoactive hormones in patients with Autosomal dominant polycystic kidney disease (ADPKD) ...

Eligibility Criteria

Inclusion

  • ADPKD patients: -age \>18 years, diagnosis with ADPKD, informed consent, contraception for fertile women
  • Patients with chronic kidney disease: age \>18 years, diagnosis with chronic kidney disease other then ADPKD, informed consent, contraception for fertile women
  • Healthy volunteers: age \>18 years, healthy, informed consent, contraception for fertile women

Exclusion

  • ADPKD patients: Renal transplantation, operation in the kidney, Diabetes mellitus, neoplastic conditions, pregnancy, breastfeeding, unwillingness to participate, intolerance towards urine dilution or urine concentration test, alcohol or medical abuse, BP \>170/110 despite regulation, unacceptable side effects to background medication (antihypertensive medicine) during the trial.
  • Patients with chronic kidney disease: Renal transplantation, operation in the kidney, Diabetes mellitus, medullary cystic kidney disease, lithium nephropathy, neoplastic conditions, pregnancy, nursing, unwillingness to participate, intolerance towards urine dilution or urine concentration test, alcohol or medical abuse, BP \>170/110 despite regulation, unacceptable side effects to background medication (antihypertensive medicine) during the trial.
  • Healthy volunteers: Arterial hypertension, significant clinical signs of heart, lungs, liver, kidneys, endocrine, brain or neoplastic disorders, alcohol or drug abuse, medical treatment, smoking, pregnancy or breastfeeding, smoking, clinically significant abnormal findings in blood, urine tests or electrocardiogram, blood donation within the last month before the examination date in the first trial sequence, intolerance to or unacceptable side effects of urine concentration and urine dilution test

Key Trial Info

Start Date :

September 25 2017

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 20 2020

Estimated Enrollment :

51 Patients enrolled

Trial Details

Trial ID

NCT04363554

Start Date

September 25 2017

End Date

April 20 2020

Last Update

April 30 2020

Active Locations (1)

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1

Department of Medical Research, Regional Hospital Holstebro

Holstebro, Denmark, 7500