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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02752841
Other study ID # 879658-1
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date May 1, 2016
Est. completion date May 31, 2019

Study information

Verified date July 2019
Source Brown University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Examine the effect of nutritional vitamin D repletion on urinary calcium excretion and kidney stone burden in calcium kidney stone formers


Description:

The investigators plan to conduct a clinic-based interventional study of 50 patients followed at Miriam Hospital Kidney Stone Clinic with history of nephrolithiasis, urinary calcium excretion between 150 and 400 mg/day, and 25-vitamin D deficiency/insufficiency (defined as serum level ≤ 30ng/ml). The intervention is oral ergocalciferol 50,000 IU per week for 12 weeks (repletion course). After that, the same repletion course will be repeated if serum 25-vitamin D remains ≤ 30ng/ml or drops to ≤ 30ng/ml anytime during the study. Otherwise, a maintenance dose of cholecalciferol 1,000 IU daily or ergocalciferol 50,000 IU monthly will be prescribed for the rest of the study. Each participant will serve as his own control. The outcome is the change in urinary calcium excretion and stone burden assessed by renal ultrasound. The planned study duration is 12 months. The investigators will have greater than 95% power to detect a 10% increase in 24-hour urinary calcium.


Recruitment information / eligibility

Status Terminated
Enrollment 20
Est. completion date May 31, 2019
Est. primary completion date May 31, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- History of nephrolithiasis

- 25(OH)D deficiency (defined as serum level = 30ng/ml) within 3 months of enrollment

- 24-hour urinary calcium excretion > 150 mg/day and < 400 mg/day (measured less than 2 months prior to study enrollment)

Exclusion Criteria:

- Known uric acid, cystine, or struvite stone disease

- Hypercalcemia (serum calcium >10.4 mg/dl within the past 12 months)

- Gross hematuria within the past 6 months

- Acute stone event within the past 1 month

- Recent stone intervention within the past 1 month

- Suspected or known secondary causes of hypercalciuria such as primary hyperparathyroidism, sarcoidosis, hyperthyroidism, or malignancy (except non-melanoma skin cancer)

- Addition or dose change of medicines potentially affecting urinary calcium since enrollment 24-hour urine collection (including diuretics, magnesium supplements, potassium supplements, potassium citrate, and vitamin D supplementation)

- Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Nutritional vitamin D repletion and maintenance
Ergocalciferol (50,000 IU weekly for 12 weeks) for vitamin D repletion, ergocalciferol (50,000 IU monthly) or cholecalciferol (1000 IU daily) for maintenance of vitamin D

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Brown University

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in urinary calcium excretion measured by timed urine collection Examine changes in urine calcium excretion at the end of the 12month study. Urinary calcium excretion are measured by 24-hour urine collections for calcium (mg per day), and the differences are the changes of 24-hour urine calcium (mg per day) between those measured at month 12 and at the enrollment Baseline and 12 months
Secondary Changes in kidney stone burden measured by ultrasound Changes in kidney stone burden at the end of the 12month study. Total stone burden is calculated by number of stones x stone sizes, i.e., patient A has one stone measured at 2 mm and two stones measured at 3 mm, then total stone burden = 1x2 +2x3=8mm. Baseline and 12 months
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