Dent's DiseasePhase 2/3DESYNCT00638482
Dose-Dependent Effect of Thiazide in Dent's Disease Hypercalciuria
A Phase 2/3 study testing Hydrochlorothiazide in people with Dent's Disease and Nephrolithiasis, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 3 to 18 years, men only
- Conditions the study is for
- Dent's Disease, Nephrolithiasis
- What is being tested?
- Hydrochlorothiazide
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 10 participants
- Where
- 1 siteFrance
- Study dates
- Jul 2003to Dec 2005
- Phase
- Phase 2/3
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 3 to 18 years
- Men only
- No healthy volunteers
- Child, Adult
Who may be able to join
- Children > 3 yrs old who met at least three standard criteria for Dent's 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.
- Dent's Disease confirmed by direct sequencing of the CLCN5 gene according to Lloyd et al.
Who cannot join
- 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.
- Overt renal loss of sodium
- Inability to adapt to severe sodium restriction
Trial locations and contacts
1 site in 1 country.
France1 site
Centre d'investigation clinique HOPITAL GEORGE POMPIDOU
Paris, 75015
About this study
Official title: Pharmacodynamic Evaluation of the ANTICALCIURIC Effect of Hydrochlorothiazide in Dent's Disease
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.
Read the 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.
- Conditions
- Dent's Disease, Nephrolithiasis
- Being tested
- Hydrochlorothiazide
- Keywords
- Dent's disease, Nephrolithiasis, clinical trial, thiazides
- Medical subject headings
- Dent Disease, Nephrolithiasis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
HydrochlorothiazideDrug
Hydrochlorothiazide
| Study group | Role | What they receive |
|---|---|---|
| 1 | Experimental | Hydrochlorothiazide Receives: Drug: Hydrochlorothiazide |
What is being measured
The primary outcome is the main question the study is designed to answer.
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
Measured: 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,
Secondary outcomes (2)
clinical events (cramps, symptomatic dehydration, acute weight loss)
Measured: 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)
Measured: at least two times overall the study, at J15 and at the end of each period.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted19 Mar 2008 (estimated)
- Study startJul 2003
- Primary completionDec 2005
- Study completionDec 2005
Why it stopped: terminated
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Dent's DiseaseStudies of the same condition, open and under way.
- More trials run by Assistance Publique - Hôpitaux de ParisThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2/3
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 10 participants (actual)
Sponsor and investigators
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Sponsor type
- University, hospital or other
- Investigators
- Anne BLANCHARD, MD PhD, Principal investigator, Assistance Publique - Hôpitaux de Paris
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00638482
- Sponsor's protocol ID
- P011114
- Other IDs
- AOM 1093
- Acronym
- DESY
- Status last verified
- Jul 2003
- First submitted
- 12 Mar 2008
- Last updated
- 19 Mar 2008
- Results posted
- No
- Data monitoring committee
- No
Publications
Blanchard A, Vargas-Poussou R, Peyrard S, Mogenet A, Baudouin V, Boudailliez B, Charbit M, Deschesnes G, Ezzhair N, Loirat C, Macher MA, Niaudet P, Azizi M. Effect of hydrochlorothiazide on urinary calcium excretion in dent disease: an uncontrolled trial. Am J Kidney Dis. 2008 Dec;52(6):1084-95. doi: 10.1053/j.ajkd.2008.08.021. Epub 2008 Oct 30.
PubMed 18976849
Study at a glance
From the registry record, last updated by the sponsor on 19 Mar 2008. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pharmacodynamic Evaluation of the ANTICALCIURIC Effect of Hydrochlorothiazide in Dent's Disease
- ClinicalTrials.gov ID
- NCT00638482
- Acronym / sponsor ID
- DESY / P011114
- Conditions
- Dent's Disease, Nephrolithiasis
- Keywords
- Dent's disease, Nephrolithiasis, clinical trial, thiazides
- Phase
- Phase 2/3
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: terminated
- Enrolment
- 10 participants (actual)
- Lead sponsor
- Assistance Publique - Hôpitaux de ParisUniversity, hospital or other
- Study start
- Jul 2003
- Primary completion
- Dec 2005 (actual)
- Study completion
- Dec 2005 (actual)
- First posted
- 19 Mar 2008 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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 design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| 1 | Experimental | Drug: HydrochlorothiazideHydrochlorothiazide |
Who may qualify
- Ages
- 3 to 18 years
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (2 listed)
- Children > 3 yrs old who met at least three standard criteria for Dent's 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.
- Dent's Disease confirmed by direct sequencing of the CLCN5 gene according to Lloyd et al.
Key exclusion criteria (3 listed)
- 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.
- Overt renal loss of sodium
- Inability to adapt to severe sodium restriction
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| HydrochlorothiazideHydrochlorothiazide | Drug | 1 |
Primary outcome
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,
2 secondary outcomes
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.
Results and safety
The study was stopped early (reason given: terminated). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Mar 2008.
- Derived from this study: PubMed 18976849Blanchard A, Vargas-Poussou R, Peyrard S, Mogenet A, Baudouin V, Boudailliez B, Charbit M, Deschesnes G, Ezzhair N, Loirat C, Macher MA, Niaudet P, Azizi M. Effect of hydrochlorothiazide on urinary calcium excretion in dent disease: an uncontrolled trial. Am J Kidney Dis. 2008 Dec;52(6):1084-95. doi: 10.1053/j.ajkd.2008.08.021. Epub 2008 Oct 30.
Related trials for Dent's Disease
Active, not recruitingObservational study
Ultrasound for Socket Healing Evaluation
Healing Wound, Alveolar; Wound
RecruitingObservational study
Prospective Research Rare Kidney Stones (ProRKS)
Hyperoxaluria, Cystinuria
RecruitingObservational study
Rare Kidney Stone Consortium Biobank
Primary Hyperoxaluria, Dent Disease
RecruitingObservational study
Rare Kidney Stone Consortium Patient Registry
Primary Hyperoxaluria, Dent Disease
RecruitingObservational study
Monogenic Kidney Stone - Genetic Testing
Rare Kidney Stone Diseases
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Anne BLANCHARD, MD PhD principal investigator
Assistance Publique - Hôpitaux de Paris
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2/3 study testing Hydrochlorothiazide in people with Dent's Disease and Nephrolithiasis, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 19 Mar 2008. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this combined phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: terminated). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
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,). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00638482, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Mar 2008; AzTrials last refreshed its copy on 6 Nov 2026.