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Trial registered on ANZCTR
Registration number
ACTRN12613000848707
Ethics application status
Approved
Date submitted
20/04/2013
Date registered
1/08/2013
Date last updated
8/08/2013
Type of registration
Retrospectively registered
Titles & IDs
Public title
Effects of Magnesium supplementation on metabolic control in type 2 diabetic subjects
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Scientific title
A randomised, placebo-controlled, double-blind, cross-over study of the effects of Magnesium supplementation on metabolic control in type 2 diabetic patients
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Secondary ID [1]
282318
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None
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Universal Trial Number (UTN)
U1111-1141-8501
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Trial acronym
None
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Diabetes
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Metabolic control
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Condition category
Condition code
Metabolic and Endocrine
289204
289204
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0
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Diabetes
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
One hundred diabetic patients were randomly assigned to receive two tablets Magnesium lactate 3.7 mmol (n=50) twice a day or placebo (n=50) during three months. After a washout period of three months each patient was then treated with the alternative regimen for an additional three months period. The treatment adherence will be assessed by measuring the urinary Magnesium clearance and counting the tablets taken after each intervention period. The difference will be calculated as a percentage of the number that should have been taken. Non-adherence (<80% or >120%) will be treated as protocol violation.
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Intervention code [1]
286933
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Treatment: Drugs
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Comparator / control treatment
Placebo will be taken in the same frequency as the intervention treatment.
The placebo tablet will have the same outward appearance as the intervention tablet.
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Glycemic control as evaluated by glycated hemoglobin and fast glycemia
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Assessment method [1]
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Timepoint [1]
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At baseline and after every intervention period
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Secondary outcome [1]
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Insulin resistance estimated according to the Homeostasis Model Assessment (HOMA)
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Assessment method [1]
302230
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Timepoint [1]
302230
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At baseline and after every intervention period
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Eligibility
Key inclusion criteria
1. Type 2 diabetics with less than 15 years diagnosed.
2. Under treatment with diet, excercise or oral hypoglycemic agents.
3.- Adequate renal function
4.- Absence of any type of cancer
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Minimum age
18
Years
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Maximum age
70
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. Chronic kidney failure
2. Use of diuretics
3. Chronic diarrhea
4. Alcoholism
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
The subjects will be recruited from those receiving attention in the diabetic clinic of Familial Medicine Unit 43 of the Mexican Social Security Institute. Subjects will be randomly assigned to receive Magnesium or placebo. Concealment by allocation schedule held independently by central administration staff.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Randomization was achieved by the use of a computerised sequence generation
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Crossover
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
The primary endpoint was glycated haemoglobin. For detecting a difference of 10% or more between the two treatments with a power of 0.8 and a = 0.05, patients group size was calculated at 30. However 50 subjects by group will be selected to allow for non-compliance to therapy and assuming a dropout of 40%. Differences between groups will be estimated by two tailed paired Student t or Mann- Whitney test. Chi-squared test will be used for categoric variables. Differences will be considered to be statistically significant for P values lower than 0.05. Statistical analyses will be performed using SPSS IBM V 18 software.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/04/2012
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Actual
1/05/2012
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Date of last participant enrolment
Anticipated
1/08/2012
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Actual
10/08/2012
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
100
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
5023
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Mexico
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State/province [1]
5023
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Tabasco
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Universidad Juarez Autonoma de Tabasco
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Address [1]
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Av. Universidad S/N
Zona de la Cultura
Colonia Magisterial C.P. 86040
Villahermosa, Centro, Tabasco
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Country [1]
287130
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Mexico
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Primary sponsor type
Hospital
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Name
Hospital General de Zona No 46. Instituto Mexicano del Seguro Social
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Address
Carretera Villahermosa-Frontera SN.
Colonia Casa Blanca 86090
Villahermosa, Tabasco
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Country
Mexico
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
285901
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Country [1]
285901
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Comite Local de Investigacion en Salud 2701
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Ethics committee address [1]
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Hospital General de Zona No 2 Francisco Trujillo Gurria SN Colonia Pueblo Nuevo Cardenas Tabasco C.P. 86500
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Ethics committee country [1]
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Mexico
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Date submitted for ethics approval [1]
289135
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Approval date [1]
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18/01/2012
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Ethics approval number [1]
289135
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R-2012-2701-1
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Summary
Brief summary
This is a randomized, placebo-controlled, double blind, cross-over study to investigate the effects of Magnesium supplementation on metabolic control in type 2 diabetic patients. A group of 100 patients were iniitially selected and divided to receive two tablets Magnesium lactate 3.7 mmol twice a day (n=50) or placebo (n=50) during three months. After a washout period of three months, each patient was then treated with the alternatively regimen for an additional three months period. Glycemia,glycated hemoglobin, insulin, serum Magnesium and urine Magnesium excretion and other routine biochemical parameters will be performance at the baseline and after intervention period. Comparison between groups will be carried out by the paired Student t test or Mann Whitney test.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Jorge Luis Ble Castillo
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Address
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UNIVERSIDAD JUAREZ AUTONOMA DE TABASCO
PROFESSOR-RESEARCHER
AV GREGORIO MENDEZ 2838-A
COLONIA TAMULTE DE LAS BARRANCAS 86150
VILLAHERMOSA, TABASCO
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Country
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Mexico
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Phone
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(+52) 993 3145466
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Adrian Navarrete Cortes
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Address
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MEDICO NO-FAMILIAR (MEDICINA INTERNA)
INSTITUTO MEXICANO DEL SEGURO SOCIAL
AV UNIVERSIDAD S/N
COLONIA CASA BLANCA
VILLAHERMOSA TABASCO 86060
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Country
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Mexico
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Phone
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(+52) 993 3517929
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Fax
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Email
39215
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[email protected]
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Contact person for scientific queries
Name
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Jorge Luis Ble Castillo
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Address
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UNIVERSIDAD JUAREZ AUTONOMA DE TABASCO
PROFESSOR-RESEARCHER
AV GREGORIO MENDEZ 2838-A
COLONIA TAMULTE DE LAS BARRANCAS 86150
VILLAHERMOSA, TABASCO
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Country
39216
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Mexico
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Phone
39216
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(+52) 993 3145466
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Fax
39216
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Email
39216
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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