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Vitamin B Complex and Diabetic Nephropathy in Type 1 Diabetes

The Role of Vitamin B Complex as an Adjuvant Therapy for Diabetic Nephropathy in Pediatric Patients With Type 1 Diabetes

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03594240
Enrollment
80
Registered
2018-07-20
Start date
2017-03-01
Completion date
2018-04-02
Last updated
2018-07-20

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

Conditions

HbA1c Level, Plasma Homocysteine

Brief summary

Homocysteine levels have been found elevated in T1DM patients with Diabetic nephropathy (DN) due to several causes, including dietary deficiencies. Hyperhomocysteinemia induces renal injury and is associated with increasing urinary albumin excretion(UAE). Therefore, the investigators performed a randomized-controlled trial of oral supplementation with vitamin B complex as an adjuvant therapy for nephropathy in pediatric patients with T1DM and assessed its relation to homocysteine levels, glycemic control, microalbuminuria and cystatin C as a marker of nephropathy.

Detailed description

This trial included 80 vitamin B12-deficient T1DM patients with nephropathy, despite oral angiotensin-converting enzyme inhibitors . Enrolled patients aged 12-18 years with at least 5 years disease duration and HbA1c ≤8.5%. Patients were randomly assigned into two groups; intervention group who received vitamin B complex once daily orally . The other group did not receive any supplementation and served as a control group. Both groups were followed-up for 12 weeks with assessment of plasma homocysteine, HbA1c, cystatin C and UAE.

Interventions

Vitamin B complex tablets (Neurorubine TM -Forte Lactab TM) once daily

DIETARY_SUPPLEMENTPlacebo

Patients in placebo group received placebo that were similar in appearance to Vitamin B complex tablets and the administered dose was as the same schedule as Vitamin B complex.

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Intervention model description

Patients were randomly assigned into two groups; intervention group who received vitamin B complex once daily orally and control group who did not receive B complex

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Patients with type 1 diabetes. * Patients aged 12-18 years with at least 5 years disease duration. * Active diabetic nephropathy in the form of microalbuminuria (urinary albumin excretion \[UAE\] 30-299 mg/g creatinine in two of three samples over a 3- to 6- months period despite angiotensin converting enzyme inhibitors) * Hemoglobin A1c (HbA1c) ≤8.5% * Patients on regular visit to clinic. * Patients on regular insulin therapy.

Exclusion criteria

Patients were excluded if they have any of the following: * Patients with history of liver disease or any disorder likely to impair liver functions or elevated liver enzymes. * Patients with any evidence of renal impairment due to cause other than diabetes. * Patients with hypertension. * Hepatitis virus infection (B or C) or any evidence of infection. * Taking any vitamins or food supplements one month before study. * Participation in a previous investigational drug study within 3 months preceding screening.

Design outcomes

Primary

MeasureTime frameDescription
Change in plasma homocysteine12 weeksChange in plasma homocysteine level after 12 weeks of oral vitamin B complex intake

Secondary

MeasureTime frameDescription
Change in HbA1c level12 weeksChange in HbA1c level after 12 weeks of oral vitamin B complex intake

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026