Randomized Double-blind Placebo-controlled Trial Assessing the Efficacy of Standard and Low Dose Hydrochlorothiazide Treatment in the Prevention of Recurrent Nephrolithiasis (NOSTONE)
Primary Purpose
Nephrolithiasis
Status
Completed
Phase
Phase 3
Locations
Switzerland
Study Type
Interventional
Intervention
Placebo oral capsule
12.5 mg hydrochlorothiazide
25.0 mg hydrochlorothiazide
50.0 mg hydrochlorothiazide
Sponsored by
About this trial
This is an interventional prevention trial for Nephrolithiasis focused on measuring kidney stones, hydrochlorothiazide
Eligibility Criteria
Inclusion Criteria:
- Informed Consent as documented by signature
- Age 18 years or older
- Recurrent kidney stone disease (≥ 2 stone events within the last 10 years prior to randomization)
- Any past kidney stone containing 50% or more of calcium oxalate, calcium phosphate or a mixture of both
Exclusion Criteria:
- Pharmacologic prevention for stone recurrence less than 3 months prior to randomization
Patients with secondary causes of recurrent calcareous nephrolithiasis including:
- Severe eating disorders (anorexia or bulimia)
- Chronic inflammatory bowel disease, bariatric surgery, intestinal surgery with malabsorption or chronic diarrheal status
- Sarcoidosis
- Primary hyperparathyroidism
- Complete distal tubular acidosis
- Active malignancy
Patients with the following medications:
- Thiazide or loop diuretics
- Carbonic anhydrase inhibitors (including topiramate)
- Xanthine oxidase inhibitors (febuxostat or allopurinol)
- Alkali, including potassium citrate or sodium bicarbonate
- Treatment with 1,25-OH Vitamin D (calcitriol)
- Calcium supplementation
- Bisphosphonates
- Denosumab
- Teriparatide
- Glucocorticoids
- Obstructive uropathy, if not treated successfully
- Urinary tract infection, if not treated successfully
- Chronic kidney disease (defined as CKD-EPI eGFR < 30 mL/min per 1,73 m2 body surface area for more than 3 months)
- Patients with a kidney transplant
- > 3 gout arthritis episodes within one year prior to randomisation or gout arthritis requiring uric acid lowering therapy
- Cystinuria at screening
- Hypokalemia (blood potassium level < 3 mmol/L) at screening
- Hyponatremia (blood sodium level < 125 mmol/L) at screening
- Pregnant and lactating women [pregnancy test to be performed for women of child-bearing potential (defined as women who are not surgically sterilized/ hysterectomized, and/ or who are postmenopausal for less than 12 months)]
- Previous (within 3 months prior to randomization) or concomitant participation in another interventional clinical trial
- Inability to understand and follow the protocol
- Known allergy to the study drug
Sites / Locations
- Kantonsspital Aarau
- University Hospital Basel
- Ospedale Regionale di Bellinzona e Valli (San Giovanni)
- Bern University Hospital (Inselspital)
- Kantonsspital Graubünden
- Hôpitaux universitaires de Genève (HUG)
- Centre hospitalier universitaire vaudois (CHUV)
- Ospedale Regionale di Lugano (Civico)
- Luzerner Kantonsspital
- Hôpital de Sion
- Kantonsspital St. Gallen
- University Hospital Zürich
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Placebo Comparator
Experimental
Experimental
Experimental
Arm Label
Placebo
12.5 mg hydrochlorothiazide
25.0 mg hydrochlorothiazide
50.0 mg hydrochlorothiazide
Arm Description
Once daily for 3 years
Once daily for 3 years
Once daily for 3 years
Once daily for 3 years
Outcomes
Primary Outcome Measures
Number of stone recurrences
Composite of symptomatic or radiological recurrences
Secondary Outcome Measures
Number of symptomatic stone recurrences
Number of radiologic stone recurrences
Measured by low-dose CT
Full Information
NCT ID
NCT03057431
First Posted
February 15, 2017
Last Updated
February 8, 2023
Sponsor
Insel Gruppe AG, University Hospital Bern
1. Study Identification
Unique Protocol Identification Number
NCT03057431
Brief Title
Randomized Double-blind Placebo-controlled Trial Assessing the Efficacy of Standard and Low Dose Hydrochlorothiazide Treatment in the Prevention of Recurrent Nephrolithiasis
Acronym
NOSTONE
Official Title
Randomized Double-blind Placebo-controlled Trial Assessing the Efficacy of Standard and Low Dose Hydrochlorothiazide Treatment in the Prevention of Recurrent Nephrolithiasis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
March 9, 2017 (Actual)
Primary Completion Date
December 3, 2021 (Actual)
Study Completion Date
April 30, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The investigators plan to assess the efficacy of standard and low dose HCTZ treatment in the recurrence prevention of calcium-containing kidney stones. More specifically, the investigators aim to assess the dose-response relationship for three different dosages of HCTZ.
Study intervention: HCTZ 12.5 mg, 25 mg or 50 mg once daily per os for 24 or 36 months. In addition, all patients in HCTZ treatment arms will receive state-of-the-art non-pharmacologic recommendations for stone prevention according to current guidelines.
Control intervention: Placebo once daily per os for 24 to 36 months. In addition, all patients in the placebo arm will receive state-of-the-art non-pharmacologic recommendations for stone prevention according to current guidelines.
Detailed Description
Nephrolithiasis is a global healthcare problem with a current lifetime risk of 18.8% in men and 9.4% in women. Without specific treatment, 5- and 20-year recurrence rates are 40% and 75%, respectively. Given the high cost of medical treatments and surgical interventions as well as the morbidity related to symptomatic stone disease, medical prophylaxis for stone recurrence is an attractive approach.
About 80-90% of stones are composed of calcium oxalate with various admixtures of calcium phosphate. Increased excretion of calcium in the urine, hypercalciuria, is the most common metabolic abnormality encountered in patients with recurrent nephrolithiasis. Thiazide diuretics have been the cornerstone of pharmacologic metaphylaxis for more than 40 years. The effect of thiazides to reduce the risk of stone recurrence has been attributed to their ability to decrease urinary calcium excretion. However, other factors, such as reduction of urinary pH and urinary oxalate excretion, probably contribute to this effect. Efficacy of thiazides on recurrence prevention of calcareous nephrolithiasis was tested in 11 randomized controlled trials (RCTs). With the exception of two trials, thiazides significantly reduced stone recurrence. Most of these trials are from the 1980's and 90's and the cumulative number of patients studied is remarkably low for such a prevalent disease. Our systematic review of these RCTs revealed major methodological deficiencies in all trials, including: lack of double-blinding and intention-to-treat analysis, unclear allocation concealment, lack of adverse event and drop out reporting and unknown baseline risk of disease severity. Furthermore, high doses of thiazides were employed in all trials, in the case of the best studied thiazide, hydrochlorothiazide (HCTZ), up to 100 mg daily. At such high doses, side effects occur frequently. Nowadays, thiazides are widely used in the treatment of recurrent nephrolithiasis and arterial hypertension, but at significantly lower doses. In the case of recurrent nephrolithiasis, however, this practice is not supported by randomized evidence and consequently, the investigators do not know whether the currently employed low dose thiazide regimens are effective in reducing the risk for stone recurrence.
Thus, evidence for benefits and harms of thiazide diuretics in the prevention of calcium-containing kidney stones in general remains unclear. In addition, the efficacy of the currently employed low dose thiazide regimens to prevent stone recurrence is not known.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nephrolithiasis
Keywords
kidney stones, hydrochlorothiazide
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
416 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Once daily for 3 years
Arm Title
12.5 mg hydrochlorothiazide
Arm Type
Experimental
Arm Description
Once daily for 3 years
Arm Title
25.0 mg hydrochlorothiazide
Arm Type
Experimental
Arm Description
Once daily for 3 years
Arm Title
50.0 mg hydrochlorothiazide
Arm Type
Experimental
Arm Description
Once daily for 3 years
Intervention Type
Drug
Intervention Name(s)
Placebo oral capsule
Intervention Description
Once daily for 3 years
Intervention Type
Drug
Intervention Name(s)
12.5 mg hydrochlorothiazide
Intervention Description
Once daily for 3 years
Intervention Type
Drug
Intervention Name(s)
25.0 mg hydrochlorothiazide
Intervention Description
Once daily for 3 years
Intervention Type
Drug
Intervention Name(s)
50.0 mg hydrochlorothiazide
Intervention Description
Once daily for 3 years
Primary Outcome Measure Information:
Title
Number of stone recurrences
Description
Composite of symptomatic or radiological recurrences
Time Frame
After 3 years
Secondary Outcome Measure Information:
Title
Number of symptomatic stone recurrences
Time Frame
After 3 years
Title
Number of radiologic stone recurrences
Description
Measured by low-dose CT
Time Frame
After 3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Informed Consent as documented by signature
Age 18 years or older
Recurrent kidney stone disease (≥ 2 stone events within the last 10 years prior to randomization)
Any past kidney stone containing 50% or more of calcium oxalate, calcium phosphate or a mixture of both
Exclusion Criteria:
Pharmacologic prevention for stone recurrence less than 3 months prior to randomization
Patients with secondary causes of recurrent calcareous nephrolithiasis including:
Severe eating disorders (anorexia or bulimia)
Chronic inflammatory bowel disease, bariatric surgery, intestinal surgery with malabsorption or chronic diarrheal status
Sarcoidosis
Primary hyperparathyroidism
Complete distal tubular acidosis
Active malignancy
Patients with the following medications:
Thiazide or loop diuretics
Carbonic anhydrase inhibitors (including topiramate)
Xanthine oxidase inhibitors (febuxostat or allopurinol)
Alkali, including potassium citrate or sodium bicarbonate
Treatment with 1,25-OH Vitamin D (calcitriol)
Calcium supplementation
Bisphosphonates
Denosumab
Teriparatide
Glucocorticoids
Obstructive uropathy, if not treated successfully
Urinary tract infection, if not treated successfully
Chronic kidney disease (defined as CKD-EPI eGFR < 30 mL/min per 1,73 m2 body surface area for more than 3 months)
Patients with a kidney transplant
> 3 gout arthritis episodes within one year prior to randomisation or gout arthritis requiring uric acid lowering therapy
Cystinuria at screening
Hypokalemia (blood potassium level < 3 mmol/L) at screening
Hyponatremia (blood sodium level < 125 mmol/L) at screening
Pregnant and lactating women [pregnancy test to be performed for women of child-bearing potential (defined as women who are not surgically sterilized/ hysterectomized, and/ or who are postmenopausal for less than 12 months)]
Previous (within 3 months prior to randomization) or concomitant participation in another interventional clinical trial
Inability to understand and follow the protocol
Known allergy to the study drug
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Fuster, Prof MD
Organizational Affiliation
Division of Nephrology and Hypertension, Bern University Hospital, Bern, Switzerland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kantonsspital Aarau
City
Aarau
ZIP/Postal Code
5001
Country
Switzerland
Facility Name
University Hospital Basel
City
Basel
ZIP/Postal Code
4031
Country
Switzerland
Facility Name
Ospedale Regionale di Bellinzona e Valli (San Giovanni)
City
Bellinzona
ZIP/Postal Code
6500
Country
Switzerland
Facility Name
Bern University Hospital (Inselspital)
City
Bern
ZIP/Postal Code
3010
Country
Switzerland
Facility Name
Kantonsspital Graubünden
City
Chur
ZIP/Postal Code
7000
Country
Switzerland
Facility Name
Hôpitaux universitaires de Genève (HUG)
City
Geneve
ZIP/Postal Code
1205
Country
Switzerland
Facility Name
Centre hospitalier universitaire vaudois (CHUV)
City
Lausanne
ZIP/Postal Code
1011
Country
Switzerland
Facility Name
Ospedale Regionale di Lugano (Civico)
City
Lugano
ZIP/Postal Code
6900
Country
Switzerland
Facility Name
Luzerner Kantonsspital
City
Luzern
ZIP/Postal Code
6000
Country
Switzerland
Facility Name
Hôpital de Sion
City
Sion
ZIP/Postal Code
1951
Country
Switzerland
Facility Name
Kantonsspital St. Gallen
City
St.Gallen
ZIP/Postal Code
9007
Country
Switzerland
Facility Name
University Hospital Zürich
City
Zurich
ZIP/Postal Code
8091
Country
Switzerland
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30526528
Citation
Dhayat NA, Faller N, Bonny O, Mohebbi N, Ritter A, Pellegrini L, Bedino G, Schonholzer C, Venzin RM, Husler C, Koneth I, Del Giorno R, Gabutti L, Amico P, Mayr M, Odermatt U, Buchkremer F, Ernandez T, Stoermann-Chopard C, Teta D, Rintelen F, Roumet M, Irincheeva I, Trelle S, Tamo L, Roth B, Vogt B, Fuster DG. Efficacy of standard and low dose hydrochlorothiazide in the recurrence prevention of calcium nephrolithiasis (NOSTONE trial): protocol for a randomized double-blind placebo-controlled trial. BMC Nephrol. 2018 Dec 10;19(1):349. doi: 10.1186/s12882-018-1144-6.
Results Reference
derived
Learn more about this trial
Randomized Double-blind Placebo-controlled Trial Assessing the Efficacy of Standard and Low Dose Hydrochlorothiazide Treatment in the Prevention of Recurrent Nephrolithiasis
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