Wishing to Decrease Aquaresis in ADPKD Patients Treated With a V2Ra; the Effect of Regulating Protein and Salt
NCT ID: NCT04310319
Last Updated: 2020-11-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
12 participants
INTERVENTIONAL
2020-09-07
2021-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
TRIPLE
Study Groups
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Normal salt, low protein treatment period
6 grams of sodium chloride daily / Placebo
Sodiumchloride
Subjects will receive 4 capsules containting 750 NaCl each 2dd, making a total of 6 grams NaCl per day.
Placebo comparator (protein)
Subjects will receive 2dd 40 ml of placebo beverage (identical to protein beverage).
Normal salt, normal protein treatment period
6 grams of sodium chloride daily / 40 grams of protein daily
Sodiumchloride
Subjects will receive 4 capsules containting 750 NaCl each 2dd, making a total of 6 grams NaCl per day.
Protein
Subjects will receive 2dd 40 ml of a protein beverage containing 0.5 grams of protein per ml, making a total of 40 grams of protein per day.
Low salt, low protein treatment period
Double placebo
Placebo comparator (salt)
Subjects will receive 4 placebo capsules (identical to salt capsules) 2dd.
Placebo comparator (protein)
Subjects will receive 2dd 40 ml of placebo beverage (identical to protein beverage).
Low salt, normal protein treatment period
Placebo / 40 grams of protein daily
Protein
Subjects will receive 2dd 40 ml of a protein beverage containing 0.5 grams of protein per ml, making a total of 40 grams of protein per day.
Placebo comparator (salt)
Subjects will receive 4 placebo capsules (identical to salt capsules) 2dd.
Interventions
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Sodiumchloride
Subjects will receive 4 capsules containting 750 NaCl each 2dd, making a total of 6 grams NaCl per day.
Protein
Subjects will receive 2dd 40 ml of a protein beverage containing 0.5 grams of protein per ml, making a total of 40 grams of protein per day.
Placebo comparator (salt)
Subjects will receive 4 placebo capsules (identical to salt capsules) 2dd.
Placebo comparator (protein)
Subjects will receive 2dd 40 ml of placebo beverage (identical to protein beverage).
Eligibility Criteria
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Inclusion Criteria
2. Stable treatment regimen of tolvaptan as part of routine clinical care in the highest dose tolerable (preferably 120 mg daily), with a urine osmolality lower than 250 mosmol/L.
3. Age \>= 18 years.
4. eGFR \>30 ml/min/1.73m2.
5. Providing informed consent.
6. Compliance to the recommended diet at two consecutive times.
Exclusion Criteria
2. Patients who are unlikely to adequately comply to the trial's procedures (due for instance to medical conditions likely to require interruption or discontinuation, history of substance abuse or non-compliance).
3. a. Patients taking medication likely to confound endpoint assessments:
* lithium in any dosing regimen;
* chronic use of systemic corticosteroids in any dosage;
* chronic use of any diuretics in any dosing regimen;
* daily use of any NSAIDs in any dosing regimen;
3\. b. Patients having concomitant illnesses likely to confound endpoint assessments (e.g. diabetes mellitus for which medication is needed or diabetes insipidus).
4\. Women who are pregnant or breastfeeding. 5. Patients with a blood pressure over 160/100 mm Hg at baseline.
18 Years
ALL
No
Sponsors
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Esther Meijer
OTHER
Responsible Party
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Esther Meijer
Principal Investigator, nephrologist
Principal Investigators
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Esther Meijer, Dr.
Role: PRINCIPAL_INVESTIGATOR
Universitar Medical Centre Groningen
Locations
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UMC Groningen
Groningen, , Netherlands
Countries
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Central Contacts
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References
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St Pierre K, Cashmore BA, Bolignano D, Zoccali C, Ruospo M, Craig JC, Strippoli GF, Mallett AJ, Green SC, Tunnicliffe DJ. Interventions for preventing the progression of autosomal dominant polycystic kidney disease. Cochrane Database Syst Rev. 2024 Oct 2;10(10):CD010294. doi: 10.1002/14651858.CD010294.pub3.
Other Identifiers
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NL2019WATER
Identifier Type: -
Identifier Source: org_study_id