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Evaluation of changes in urinary parameters after oral administration of magnesium chlorides and potassium citrate in pediatric with calcium oxalate urolithiasis.

Evaluation of changes in urinary parameters after oral administration of magnesium chlorides and potassium citrate in pediatric with calcium oxalate urolithiasis.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138707091282N1
Enrollment
40
Registered
2011-04-12
Start date
2008-02-02
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

urolithiasis. Calculus of kidney and ureter

Interventions

Intervention 1: Phase 1: Oral solution of potassium citrate, 0.5 cc/kg/dose, every 8 hours, 30 min after meal, for 4 weeks. Intervention 2: Phase 2: Combination of K Citrate 0.5 cc/kg/dose, every 8 ho
Treatment - Drugs
Phase 1: Oral solution of potassium citrate, 0.5 cc/kg/dose, every 8 hours, 30 min after meal, for 4 weeks
Phase 2: Combination of K Citrate 0.5 cc/kg/dose, every 8 hours, 30 min after meal as well as Mg Chloride 10-20 mg/kg/dose equivalent to 180 meq elemental Mg for 4 weeks

Sponsors

Isfahan University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
2 Years to 18 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 2-12 years with possibility of calcium oxalate kidney stone, No past history of peptic ulcer, chronic diarrhea or cardiac disease, primary hyperparathyroidism, consumption of anticonvulsants, No proven history of disorders affecting tubular ion excretion such as: recent urinary tract infection , distal renal tubular acidosis , chronic pyelonephritis, renal dysfunction and obstructive uropathy Exclusion criteria: Patients who did not complete all steps of the study, refusing to consume either potassium citrate or magnesium chloride

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood parameter (Ca-K-Na-Cl-Cit-Ox-P-Cr-Mg). Timepoint: Before and 4 weeks after intervention. Method of measurement: blood test.;Urine parameter (Ca-K-Na-Cl-Cit-Ox-P-Cr-Mg). Timepoint: Before and4 weeks after intervention. Method of measurement: 24-hour urine test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Alaleh Gheisary

Isfahan University of Medical Sciences and Health Services

gheisari@med.mui.ac.ir+98 913 313 3563

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026