Dose-Dependent Effect of Thiazide in Dent's Disease Hypercalciuria (DESY)
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|ClinicalTrials.gov Identifier: NCT00638482|
Recruitment Status : Terminated (terminated)
First Posted : March 19, 2008
Last Update Posted : March 19, 2008
|Condition or disease||Intervention/treatment||Phase|
|Dent's Disease Nephrolithiasis||Drug: Hydrochlorothiazide||Phase 2 Phase 3|
Hide Detailed Description
Intrarenal calcifications (nephrocalcinosis) is present in Dent's disease and likely contribute to progression toward renal failure. In order to prevent this complication it is usually proposed to treat affected patients during childhood with high doses of thiazides. Indeed, this class of diuretics is used for years to treat hypertension, can lower urinary calcium excretion. However the doses usually used are high, are known to be associated with adverse events such as severe potassium depletion, decrease in blood pressure and dehydration. The purpose of the study was to test whether lower dose of thiazides would be better tolerated, with similar efficacy to lower urinary calcium excretion, as previously demonstrated in other indication such as treatment of hypertension.
Patient recruitment and clinical evaluation Eight subjects with genetically proven Dent's disease were recruited through a French nationwide network for tubulopathies and were enrolled between July 2003 and December 2005.
All patients met at least three standard criteria for the disease including hypercalciuria, low molecular weight proteinuria and one of the following disorders: nephrocalcinosis, nephrolithiasis, renal failure, aminoaciduria, glucosuria, renal phosphate wasting, or familial history of Dent's disease. The disease was confirmed in all patients by direct sequencing of the CLCN5 gene according to Lloyd et al. (25) Patients presenting hyponatremia (< 135 mM), hypokalaemia (< 3.3 mM), severe fanconi syndrome, or chronic renal failure (GFR estimated with the Schwartz formula < 30 mL.min-1.1.73m-2) were excluded from the study.
The protocol was approved by the "comité de protection des personnes" (Paris, Hôtel Dieu) and all subjects and/or their parents gave written informed consent for the participation in the study.
Sodium restriction test Because a renal loss of sodium was reported in the disease, the pharmacological study was preceded by a sodium restriction test involving NaCl intake equivalent to 0.3 mmol/kg BW) and an age-adjusted calcium intake of 1200-1500 mg/day, to assess the tolerance to sodium depletion and its effect on calcium excretion. Sodium restriction was stopped after 5 days or when 24h urinary sodium excretion matched theoretical salt intake. Blood and urine samples were taken in the morning, two hours after a light calcium-free breakfast and after a 30 minute rest in the supine position on the first and last days of the low sodium diet determining electrolytes, plasma proteins, hematocrit, and plasma renin and aldosterone concentrations.
PHARMACOLOGICAL STUDY After completion of the sodium restriction test, the seven remaining patients entered a three-period, forced titration sequential open-label trial. They were instructed to follow normal sodium, isocaloric diet, with an age-adjusted calcium intake of 1200 to 1500 mg/d. One patient had a tendency to hypokalaemia (3.3 mM), requiring potassium chloride salt supplementation before entering the trial.
After a one month run-in phase, the patients received sequentially a low dose (6.25 mg/day), an intermediate dose (12.5 mg/day), and a high dose (25 mg/day) of hydrochlorothiazide (HCTZ), each dose being administered for a period of two months. Amiloride (5 mg/day) was started at the beginning of the study, and continued throughout the sequential trial to reduce the risk of HCTZ-induced hypokalaemia. For safety reasons, two patients did not receive the last 25 mg dose of HCTZ because of a body weight (BW) < 25 kg. The last HCTZ dose was followed by a one month withdrawal period (phase E).
Clinical (blood pressure and BW), biological and hormonal evaluations were conducted at baseline and at the end of each treatment period, between 9:00 and 10:00 hours, two hours after a light calcium-free breakfast and a one hour-rest in a reclined position. At the end of the baseline and washout periods and each treatment period, two successive 24-h urine collections were obtained, and a morning spot urine sample was collected on the day of investigation for measurements of urine electrolytes (Na, K, calcium) and creatinine. Hematocrit, and electrolyte, creatinine, proteins, renin and aldosterone concentrations were measured in blood samples. Additionally, Blood Pressure, Body Weight and biological tolerance was assessed 15 days after each increase in the HCTZ dose.
Analytical methods Methods for the determination of plasma sodium, potassium, creatinine, magnesium, PTH, 25-OH vitamin D, renin, aldosterone and calcitriol levels have been described elsewhere.
Statistical Methods The effects of sodium restriction and HCTZ on clinical and biological markers were first evaluated by Friedman's tests. If a global time-effect was significant, the change between baseline and the last measurement of the treatment period was tested by a Wilcoxon's paired test. All data are expressed as median range [minimum; maximum], except otherwise specified. Values of 24h-urine collection of each period used for analyses were mean of the measurements made on the two consecutive daily collections. Values for a given 24-h collection were excluded from analysis if the creatinine excretion on that collection varied by more than 15% or the sodium excretion varied by more than 25% from the mean of values for other collections by that patient.
All analyses were carried out using SAS Statistical Software (Version 8.2, Cary, NC, USA) and STATVIEW(SAS Institute Inc., Cary NC) and a p value of less than 0.05 was considered to be significant.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||10 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Pharmacodynamic Evaluation of the ANTICALCIURIC Effect of Hydrochlorothiazide in Dent's Disease|
|Study Start Date :||July 2003|
|Actual Primary Completion Date :||December 2005|
|Actual Study Completion Date :||December 2005|
- to investigate the dose-dependent benefit/risk ratio of low (6.25 mg/day), intermediate (12.5 mg/day) and high (25 mg/day) doses of hydrochlorothiazide [ Time Frame: at the end of the baseline initial and final washout periods (one month each) and at the end of each two-months duration treatment period, ]
- clinical events (cramps, symptomatic dehydration, acute weight loss) [ Time Frame: at least two times overall the study, at J15 and at the end of each period. ]
- Biological : acute renal failure (estimated GFR), hypokalemia, hyperkalemia, hyponatremia, biological signs of extra cellular dehydration (protides, hematocrit, plasma active renin, plasma aldosterone) [ Time Frame: at least two times overall the study, at J15 and at the end of each period. ]
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): NCT00638482
|Centre d'investigation clinique HOPITAL GEORGE POMPIDOU|
|Paris, France, 75015|
|Principal Investigator:||Anne BLANCHARD, MD PhD||Assistance Publique - Hôpitaux de Paris|