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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04638166
Other study ID # MINERVA
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date January 25, 2018
Est. completion date January 2021

Study information

Verified date November 2020
Source Singapore General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators would like to assess if the intake of high bicarbonate mineral water would not only increase total fluid intake but will also be able to give patients the additional benefit of correcting the urinary abnormalities which may predispose them to stone formation.


Description:

The life time risk of developing nephrolithiasis is about 10-15% in the western world, but can be as high as 20-25% in the middle east. Evidence suggests that the incidence and prevalence of kidney stones is increasing globally which represent a significant economic burden. Besides the lack of hydration, the most common metabolic abnormalities associated with calcium stones are hypercalciuria, hypocitraturia and hyperoxaluria. In addition, low urinary pH from consumption of non-dairy animal protein has been associated with reduced urinary citrate and increased uric acid stones which form a nidus for subsequent calcium oxalate precipitates. Dietary modification is the first line approach in the treatment of idiopathic calcium oxalate (CaOx) nephrolithiasis. General advice includes adequate hydration, avoiding oxalate-rich foods, and consumption of an adequate amount of calcium. Adequate hydration is an easy and effective way of preventing stones. Siener et al found in healthy men, consumption of mineral water rich in magnesium and bicarbonate resulted in favourable changes in urinary pH, magnesium and citrate excretion (inhibitors of CaOx stone formation). Our pilot study in 10 young and healthy surgical residents also revealed similar results after drinking bicarbonate rich mineral water for 1 week. In this study, the investigators compared the effect of drinking bicarbonate rich mineral water with plain water on urine biochemistry in a prospective randomized study in patients with known CaOx stones. The investigators hypothesize that the intake of bicarbonate rich mineral water, particularly at meal times, reduces stone risk via reduction in urinary oxalate through increased intestinal oxalate binding with dietary calcium. Other potential benefits of mineral water include increased urinary stone inhibitors like magnesium, citrate and alkalinisation of urine.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 58
Est. completion date January 2021
Est. primary completion date October 1, 2019
Accepts healthy volunteers No
Gender All
Age group 21 Years to 80 Years
Eligibility Inclusion Criteria: - patients with proven Calcium Oxalate (CaOx) stone (CaOx >50% by infrared spectroscopy) from Jan 2018 to Aug 2019 in Singapore General Hospital - all stone formers had suffered spontaneous passage or surgical removal of a urinary calculus during the study period. Exclusion Criteria: - presence of urinary tract infection - severe cardiovascular insufficiency - previously diagnosed causal metabolic disease such as hyperparathyroidism, renal tubular acidosis, primary hyperoxaluria, Wilson's disease, Cushing disease, osteoporosis and malignant diseases. - pregnant women - chronic intestinal diseases - history of previous bowel resection - participation in competitive sports

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mineral water
Drinking mineral water for 12 weeks
Plain water
Drinking plain water for 12 weeks

Locations

Country Name City State
Singapore Singapore General Hospital Singapore

Sponsors (1)

Lead Sponsor Collaborator
Singapore General Hospital

Country where clinical trial is conducted

Singapore, 

Outcome

Type Measure Description Time frame Safety issue
Primary changes of Tiselius Index compare Tiselius Index (24h urine analysis) at week 1, 4, 8 and 12 to baseline (week 0) 1, 4, 8 and 12 weeks
Primary changes of urinary oxalate level (mmol/24h) compare urinary oxalate level (24h urine analysis) at week 1, 4, 8 and 12 to baseline (week 0) 1, 4, 8 and 12 weeks
Secondary changes of other stone inhibitor/promoter (mmol/24h) compare Magnesium, Citrate, Sodium, Calcium, Uric Acid (24h urine analysis) at week 1, 4, 8 and 12 to baseline (week 0) 1, 4, 8 and 12 weeks
Secondary changes of urinary volume (ml/24h) compare urinary volume (24h urine analysis) at week 1, 4, 8 and 12 to baseline (week 0) 1, 4, 8 and 12 weeks
Secondary changes of urinary pH compare urinary pH (24h urine analysis) at week 1, 4, 8 and 12 to baseline (week 0) 1, 4, 8 and 12 weeks
Secondary changes of serum electrolytes (mmol/L) compare serum sodium, potassium, calcium, phosphate, bicarbonate and uric acid at baseline (week 0) and the end of the study (week 12) 12 weeks
See also
  Status Clinical Trial Phase
Not yet recruiting NCT04169165 - Patient Compliance for Metabolic Evaluation and Medical Management in Calcium Stone Patients
Recruiting NCT04669860 - Evaluating the Bacterial and Fungal Microbiome in Patients With Calcium Oxalate Urolithiasis and Renal Cell Carcinoma
Enrolling by invitation NCT01127854 - Pilot Study to Evaluate the Contribution of Gene Variants to Idiopathic Urolithiasis
Active, not recruiting NCT05081960 - Evaluating the Vitamin K2 Status of Calcium-based Stone Formers
Active, not recruiting NCT03752684 - Oxalobacter Formigenes Colonization and Urinary Oxalate Excretion N/A