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The effects of combined choline and magnesium supplementation in patients with type 2 diabetes mellitus

The effects of choline, magnesium and combined choline and magnesium supplementation on the components of inflammatory and coagulation markers in patients with type 2 diabetes mellitus

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110123005670N25
Enrollment
80
Registered
2018-03-09
Start date
2018-03-06
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

type 2 diabetes. Type 2 diabetes mellitus

Interventions

Intervention 1: Intervention group: 1 capsule of 500 mg of magnesium and 2 capsules of 500 mg of placebo per day for 60 days (Nano Kimia Health Co.). Intervention 2: Intervention group: 2 capsule of 5

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: patients with type 2 diabetes Men and women aged 60-30 years Patients who their diabetes have been controlled by glucose lowering tablets BMI=25-35 kg/m2

Exclusion criteria

Exclusion criteria: Unwillingness to cooperate patients with inflammatory diseases, allergy, MS, kidney, liver, thyroid diseases Use of insulin and corticosteroids and non-steroidal anti-inflammatory drugs and hormonal products Changes in diet and physical activity, and type or dosage of medications used during the study Pregnancy and breastfeeding Tobacco and supplement use

Design outcomes

Primary

MeasureTime frame
Fast Blood Sugar. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: Enzymatic with Commercial Kits.;Hemoglobin A1C. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: ELISA with Commercial Kits.;Insulin. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: ELISA.;Triglyceride. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: Enzymatic.;Total Cholesterol. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: Enzymatic.;HDL-Cholesterol. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: Enzymatic.;LDL-Cholesterol. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: Enzymatic.;Interleukin-6 (IL-6). Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: ELISA.;Vascular cell adhesion molecule 1 (VCAM-1). Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: ELISA.;Plasminogen activator inhibitor-1(PAI-1). Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: ELISA.;Tissue plasminogen activator(tPA). Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: ELISA.

Secondary

MeasureTime frame
Blood Pressure. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: Digital Barometer.;Weight. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: Scale.;Height. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: meter.;Body mass index(BMI). Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: Computing.;Fat percent. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: Bio impedance set.;Waist circumference. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: meter.;Hip circumference. Timepoint: before the intervention and 60 days after the start of the intervention. Method of measurement: meter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Ali Tarighat Esfanjani

Tabriz University of Medical Sciences

tarighata@tbzmed.ac.ir+98 41 3335 2292

Outcome results

None listed

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