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The effect of Biodiabetes supplement on diabetic neuropathy

Investigating the effect of probiotic supplement (biodiabet) on clinical symptoms of diabetic neuropathy: randomized clinical trial study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250111064346N1
Enrollment
60
Registered
2025-02-01
Start date
2025-01-29
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

Diabetic neuropathy. Diabetes mellitus due to underlying condition with diabetic polyneuropathy

Interventions

Intervention 1: Intervention group: After obtaining the necessary permits, the study begins. Intervention will be done for patients whose score is 7 or higher. Matching will be done according to the d

Sponsors

Yasouj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients with type 2 diabetes who have symptoms related to neuropathy. Age between 40 and 70 years old Be able to collaborate and communicate. No chronic diseases (vitamin B12 deficiency, vitamin D deficiency, folic acid deficiency, and kidney failure) Other causes that cause diabetic neuropathy will be excluded from the study, and patients who meet the inclusion criteria will be examined.

Exclusion criteria

Exclusion criteria: Having a severe physical, neurological, or psychiatric illness Taking drugs that are somehow effective in aggravating or alleviating neuropathy, such as: tricyclic antidepressants - antipsychotics - anticonvulsants (except pregabalin) and painkillers.

Design outcomes

Primary

MeasureTime frame
Diabetic neuropathy. Timepoint: Before and after the intervention. Method of measurement: Michigan Neuropathy Screening Instrument (MNSI).

Secondary

MeasureTime frame
Pain. Timepoint: Before and After the Intervention. Method of measurement: Visual Analogue Scale (VAS).;Tingling. Timepoint: Before and After the Intervention. Method of measurement: Frequency and Patient Description.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEshaq Moradi Sheibani

Yasouj University of Medical Sciences

moradishibanyisaac@yahoo.com+98 74 3334 6079

Outcome results

None listed

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