The Effect of Magnesium Oxide on Plasma Phosphate in Hemodialysis Patients

NCT ID: NCT01854437

Last Updated: 2013-05-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

42 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-06-30

Study Completion Date

2012-12-31

Brief Summary

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Hyperphosphatemia is a common problem in hemodialysis (HD) patients. Different chelators for control of Hyperphosphatemia are used. The aim of this study was to assess the effect of magnesium oxide (Mg Oxide) on the control of serum phosphorus (P) level and evaluation of its side effects in hemodialysis patients.

Detailed Description

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Conditions

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Hyperphosphatemia

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Mg Oxide

Mg Oxide (Mg®, 21st Century®) 250 mg orally for 4 weeks

Mg Oxide

Intervention Type DRUG

250 mg orally for 4 weeks

placebo

placebo 1 tab TDS

No interventions assigned to this group

Interventions

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Mg Oxide

250 mg orally for 4 weeks

Intervention Type DRUG

Other Intervention Names

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(Mg®, 21st Century®)

Eligibility Criteria

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Inclusion Criteria

hemodialysis with duration\>3 months serum P level \>5.5 mg/dl serum Ca\>8 mg/dl.

Exclusion Criteria

Mg level \>3 mg/dl
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Shiraz University of Medical Sciences

OTHER

Sponsor Role lead

Responsible Party

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Maryam Pakfetrat

associated professor of shiraz Shiraz University of Medical Sciences

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Shiraz University Hemodialysis Center

Shiraz, Fars, Iran

Site Status

Countries

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Iran

Other Identifiers

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1391

Identifier Type: -

Identifier Source: org_study_id

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