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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00784030
Other study ID # 08-774
Secondary ID
Status Active, not recruiting
Phase N/A
First received October 31, 2008
Last updated July 10, 2009
Start date November 2008
Est. completion date November 2009

Study information

Verified date July 2009
Source New York University School of Medicine
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Polycystic kidney disease (PKD) is a genetic disease that occurs in 1 in 500 individuals and leads to kidney failure in half of all affected. Currently, no treatments exist for PKD. PKD-affected kidney cells divide and multiply inappropriately, and form fluid-filled sacs called cysts. Kidney cysts continue to grow throughout life, destroying normal kidney tissue, leading to kidney failure. Based on evidence from basic science research it is believed that drinking high amounts of water can slow the abnormal cysts growth. This study aims to look at changes in urine composition with high water intake in PKD-affected persons compared to healthy individuals.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 20
Est. completion date November 2009
Est. primary completion date November 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Clinical diagnosis of Autosomal Dominant Polycystic Kidney Disease by history, ultrasound, CT or MRI

- Healthy subjects without a diagnosis of Polycystic Kidney Disease by history, ultrasound, CT or MRI

- Ages between 18 and 65

- Healthy subjects (without Polycystic Kidney Disease) must have an estimated glomerular filtration rate (eGFR by the MDRD equation) > 60 ml/min/1.73 m2 with no history of kidney disease

Exclusion Criteria:

- Women who are pregnant or nursing

- Active dependency on drugs or alcohol

- Diagnosis of syndrome of inappropriate antidiuresis

- Currently taking a vasopressin agonist or antagonist

- Blood sodium level less than < 135 mEq/L

- For healthy participants, estimated glomerular filtration rate (level of kidney function) less than < 60 ml/min/1.73 m2

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
Water
Participants will be first asked to drink 6 8-oz glasses of water over 2.5 hours on the first day, and then about 12 8-oz glasses of water over the course of the day for one week.

Locations

Country Name City State
United States New York University Langone Medical Center New York New York

Sponsors (1)

Lead Sponsor Collaborator
New York University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in urinary biomarkers One week No
See also
  Status Clinical Trial Phase
Completed NCT00571909 - Autosomal Dominant Polycystic Kidney Disease (ADPKD) Pain Study N/A
Recruiting NCT00890279 - Efficacy and Safety Study of Second-Line Treatment for Hypertension With Autosomal Dominant Polycystic Kidney Disease(ADPKD) Phase 2
Unknown status NCT00541853 - CCB Safety Study in Treatment of Hypertension of ADPKD Phase 4
Not yet recruiting NCT00067977 - Clinical Trial to Slow the Progression of ADPKD N/A