High Water Intake to Slow Progression of Polycystic Kidney Disease
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| ClinicalTrials.gov Identifier: NCT00784030 |
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Recruitment Status :
Completed
First Posted : November 2, 2008
Results First Posted : April 6, 2016
Last Update Posted : April 6, 2016
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Kidney, Polycystic, Autosomal Dominant | Other: Water | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 23 participants |
| Allocation: | Non-Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Basic Science |
| Official Title: | The Effect of Water Loading on Urinary Biomarkers |
| Study Start Date : | November 2008 |
| Actual Primary Completion Date : | May 2009 |
| Actual Study Completion Date : | May 2009 |
| Arm | Intervention/treatment |
|---|---|
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Polycystic Kidney Disease Patients
Patients who present with polycystic kidney disease (PKD)
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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. |
| Healthy Patients |
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. |
- Change in Urine cAMP Concentration and Urine Osmolality (UOsm) [ Time Frame: pre- and post-water loading (2 hours) ]Urine cAMP (UcAMP) concentration and urine osmolality UOsm) were measured pre- and post-water loading: with 2.5L over 2 hours
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| Ages Eligible for Study: | 18 Years to 65 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
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
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00784030
| United States, New York | |
| New York University Langone Medical Center | |
| New York, New York, United States, 10016 | |
| Principal Investigator: | Irina Barash, M.D. | NYU Langone Health |
| Responsible Party: | NYU Langone Health |
| ClinicalTrials.gov Identifier: | NCT00784030 |
| Other Study ID Numbers: |
08-774 |
| First Posted: | November 2, 2008 Key Record Dates |
| Results First Posted: | April 6, 2016 |
| Last Update Posted: | April 6, 2016 |
| Last Verified: | March 2016 |
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Autosomal Dominant Polycystic Kidney Disease Polycystic Kidney Disease Water Loading Biomarkers |
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Kidney Diseases Polycystic Kidney Diseases Polycystic Kidney, Autosomal Dominant Urologic Diseases Congenital Abnormalities |
Kidney Diseases, Cystic Abnormalities, Multiple Ciliopathies Genetic Diseases, Inborn |

