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Effects of Magnesium Carbonate tablet on hyperphosphatemia in patients under hemodialysis

Phase 2
Conditions
Condition 1: End stage renal disease. Condition 2: hyperphosphatemia.
End Stage Renal Disease
classified in other phosphoru metabolism defect.
E83.39
Registration Number
IRCT201105186515N1
Lead Sponsor
Vice chancellor for research, Isfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

age>18 years; serum phosphorus >5.5 mg/dl; at least 3 months on hemodialysis.
exclusion criteria: serum magnesium > 4 mg/dl; pregnancy; previous parathyroidectomy; sever hyperparathyroidism(iPTH> 500 pg/ml); Medical disease cause diarrhea; Kidney transplant; Patient Death; Non-compliance of drug usage (at least 80% of prescribed drug must be used); Drug complications making the patient unable to continue the treatment; Lost hemodialysis more than one per month or Irregular hemodialysis

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes in serum phosphorus level. Timepoint: Before trial and every 2 weeks till at the end of 6the week. Method of measurement: Lab data mg/dl.;Changes in Ca X P product. Timepoint: Before trial then every 2 weeks till the end of 6th week. Method of measurement: Lab data mg/dl.;Changes in serum calcium. Timepoint: Before trial and every two weeks till the end of 6th week. Method of measurement: Lab data mg/dl.;Changes in serum magnesium. Timepoint: Before trial and every two weeks till the end of 6th week. Method of measurement: Lab data, mg/dl.
Secondary Outcome Measures
NameTimeMethod
Abdominal pain and diarrhea. Timepoint: Before trial then every 2 weeks till the end of 6th week. Method of measurement: Clinical data(history and examination).;Cardiac arhrythmia. Timepoint: Before trial then every 2 weeks till the end of 6th week. Method of measurement: Clinical data(history and examination) and electrocardiography.;Serum LDL, HDL, Tg, Chol,. Timepoint: Before trial then at the end of 6th week. Method of measurement: Lab data mg/dl.;PTH. Timepoint: Before trial then at the end of 6th week. Method of measurement: Lab data pg/ml.;CRP. Timepoint: before trial then every 2 weeks till the end of 6th week. Method of measurement: lab data mg/l.;Serum HCo3. Timepoint: Before trial then every 2 weeks till the end of 6th week. Method of measurement: Lab data mmol/l.;Blood pressure. Timepoint: Before trial then every 2 weeks till the end of 6th week. Method of measurement: Clinical data(examination) mmHg.
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