Oral Sucrosomial® Vitamin B12 in the Management of B12 Deficiency Among Metformin-Treated Type 2 Diabetes Patients

Liaquat University of Medical & Health Sciences

Status: Enrolling

Conditions: Vitamin B 12 Deficiency; Type 2 Diabetes Mellitus (T2DM)

Treatments: Dietary Supplement: Sucrosomial® Vitamin B12; Other: Placebo (Oral)

Study type: Interventional

Funder types: Other

Identifiers

NCT06983223

LUMHS/REC/-733/09.05.2025

Details and patient eligibility

About

This randomized, double-blind, placebo-controlled clinical trial aims to evaluate the effectiveness of Sucrosomial® Vitamin B12 supplementation in the management of vitamin B12 deficiency among metformin-treated Type 2 Diabetes Mellitus (T2DM) patients. The study will compare the impact of daily Sucrosomial® B12 (1,000 mcg) versus placebo on serum vitamin B12 levels, Holo-Transcobalamin II (HoloTCII), and Transcobalamin I (TCI) levels over a 4-week period. Secondary outcomes include assessment of safety, tolerability, and glycemic control (HbA1c). Fifty participants will be randomly assigned to either the Sucrosomial® B12 or placebo group.

Full description

Vitamin B12 deficiency is a common concern in Type 2 Diabetes Mellitus (T2DM) patients, especially those treated with metformin, which is known to interfere with B12 absorption. Early identification and effective management of B12 deficiency are critical to prevent neurological and hematological complications.

This study is designed as a randomized, double-blind, placebo-controlled clinical trial to assess the efficacy of Sucrosomial® Vitamin B12 (1,000 mcg daily) compared to placebo in improving vitamin B12 status among metformin-treated T2DM patients. The study will enroll 50 participants (25 in each group) who will receive either Sucrosomial® B12 or placebo for 4 weeks.

Primary Outcome:

Change in serum vitamin B12 levels from baseline to 4 weeks.

Secondary Outcomes:

Change in Holo-Transcobalamin II (HoloTCII) levels from baseline to 4 weeks.

Change in Transcobalamin I (TCI) levels from baseline to 4 weeks.

Safety and tolerability, assessed through adverse event monitoring.

Change in glycemic control (HbA1c) from baseline to 4 weeks.

The study will include assessments at Baseline, 24 hours, 7 days, 14 days, and 30 days. Blood samples will be collected at each time point to measure vitamin B12, HoloTCII, TCI, CBC, LFTs, and RFTs. The safety profile will be monitored throughout the study.

This study will provide essential data on the effectiveness of Sucrosomial® B12 in improving vitamin B12 status among metformin-treated T2DM patients, offering a potential non-invasive intervention for managing B12 deficiency in this population.

Enrollment: 50 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adults aged 18 to 75 years.
• Diagnosed with Type 2 Diabetes Mellitus (T2DM).
• Currently on Metformin therapy for at least one year.
• Serum vitamin B12 levels below the laboratory reference range (indicating deficiency).
• Willing to provide written informed consent.
• Able to comply with study procedures and visit schedule.

Exclusion criteria

• Current or prior use of vitamin B12 supplements within the past 3 months.
• Diagnosis of pernicious anemia or other causes of vitamin B12 malabsorption (e.g., Crohn's disease, celiac disease).
• History of gastric surgery or small intestine resection.
• Use of medications known to interfere with vitamin B12 absorption (other than Metformin).
• Severe renal impairment (eGFR < 30 mL/min/1.73 m²) or end-stage renal disease.
• Severe hepatic impairment (ALT/AST > 3 times the upper limit of normal).
• Pregnant or breastfeeding women.
• Known hypersensitivity to vitamin B12 or any component of the study product.
• Participation in another clinical trial within the last 30 days.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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50 participants in 2 patient groups, including a placebo group

Sucrosomial® B12 Group

Experimental group

Description:

Participants in this group will receive Sucrosomial® Vitamin B12 (1,000 mcg), administered as an orally dissolving powder, once daily for 4 weeks. Dosage Form: Orally dissolving powder (sachet) Administration Route: Oral Frequency: Once daily Duration: 4 weeks (30 days)

Treatment:

Dietary Supplement: Sucrosomial® Vitamin B12

Placebo Group

Placebo Comparator group

Description:

Participants in this group will receive a matching placebo (identical in appearance, packaging, and taste), administered as an orally dissolving powder, once daily for 4 weeks. Dosage Form: Orally dissolving powder (sachet) Administration Route: Oral Frequency: Once daily Duration: 4 weeks (30 days)

Treatment:

Other: Placebo (Oral)