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Investigating the effect of thiamine, magnesium and vitamin D in the treatment of type 2 diabetic neuropathy

The effect of co-supplementation magnesium, thiamine and vitamin D on glycemic status and severity of neuropathy symptoms in patients with neuropathic type 2 diabetes

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191105045340N6
Enrollment
60
Registered
2025-01-19
Start date
2024-11-20
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Type 2 diabetic neuropathy. Diabetes mellitus due to underlying condition with diabetic nephropathy

Interventions

Intervention 1: Intervention group: People with type 2 diabetic neuropathy will take 2 D3fort supplements and 1 thiamine 300 mg daily for 12 weeks. Intervention 2: Control group: Subjects will receiv

Sponsors

Iran University of Medical Sciences
Lead Sponsor
Iran University of Medical Sciences
Collaborator

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Diagnosing neuropathy in people with type 2 diabetes by a doctor based on clinical symptoms (motion strength, pain intensity and paresthesia) Age range from 20 to 65 years Completion of written consent Not suffering from certain diseases such as cancer, severe kidney disease (ESRD), liver cirrhosis and autoimmune diseases.

Exclusion criteria

Exclusion criteria: Following a special diet such as ketogenic, fasting, etc. Pregnancy and breastfeeding History of persistent diarrhea or vomiting and severe gastric reflux Severe vitamin D deficiency and very high vitamin D levels

Design outcomes

Primary

MeasureTime frame
Severity of neuropathy symptoms. Timepoint: Before the start of the intervention and 12 weeks after the intervention. Method of measurement: Questionnaire based on Visual Analog Scale index (VAS index).

Secondary

MeasureTime frame
FBS. Timepoint: Before the start of the intervention and 12 weeks after the start of the intervention. Method of measurement: blood test.;Glycosylated hemoglobin A1C. Timepoint: Before the start of the intervention and 12 weeks after the start of the intervention. Method of measurement: blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Seyedeh Tayebeh Rahideh

Iran University of Medical Sciences

tayebeh_rahideh@yahoo.com+98 21 8670 1021

Outcome results

None listed

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