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The effect of vitamin k1 in diabetic patient treatment

The effect of vitamin k1 supplementation on sensitivity and insulin resistance via osteocalcin in predaibetes patients:A Randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013120915724N1
Enrollment
84
Registered
2014-01-08
Start date
2013-04-09
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

prediabetes. Abnormal glucose tolerance test

Interventions

Intervention 1: Daily consumption of one 1000 micro grams soft gel vitamin k1 for 4 weeks in intervention group. Intervention 2: Daily consumption of one softgel placebo for 4 weeks in the control gr
Prevention
Placebo
Daily consumption of one 1000 micro grams soft gel vitamin k1 for 4 weeks in intervention group.
Daily consumption of one softgel placebo for 4 weeks in the control group.

Sponsors

Vice Chancellor For Research Of Ahvaz Jundishapur University Of Medical Science, Ahvaz Jundishapur
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
22 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Willingness to participate in the study and sign the Written informed consent; Age between 22 to 45 years old; BMI=25-29.9 kg/m2; 100 =FBS=126 or 140 =2hpp=200 mg/dL Exclusion criteria: Heart, Kidney, liver and Rheumatoid diseases; Osteoporosis; Hyperthyroidism and Thyroid dysfunction; Pregnancy; Lactation; Menopause; Intake of insulin and glucose and lipid-lowering Agents; Warfarin; Corticosteroids; drugs to treat osteoporosis; Vitamin and Mineral supplements during past 6 months.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Serum carboxylated osteocalcin. Timepoint: Baseline and after 4 weeks. Method of measurement: ELISA assay.;Serum carboxylated osteocalcin. Timepoint: Baseline and after 4 weeks. Method of measurement: ELISA assay.;Serum total osteocalcin. Timepoint: Baseline and after 4 weeks. Method of measurement: ELISA assay.;Serum Hb A1C. Timepoint: Baseline and after 4 weeks. Method of measurement: HPLC assay.;Total energy and nutrient intaake. Timepoint: Baseline, middle and 4th weeks. Method of measurement: 24 hour recall.

Secondary

MeasureTime frame
Fasting and 2 hour serum insulin. Timepoint: Baseline and after 4 weeks. Method of measurement: ELISA assay.;Fasting and 2 hour serum glucose. Timepoint: Baseline and after 4 weeks. Method of measurement: calorimetric assay.;HOMA-IR. Timepoint: Baseline and after 4 weeks. Method of measurement: formula.;HOMA-%B. Timepoint: Baseline and after 4 weeks. Method of measurement: formula.;ISI. Timepoint: Baseline and after 4 weeks. Method of measurement: formula.;Serum adiponectin. Timepoint: Baseline and after 4 weeks. Method of measurement: ELISA assay.;Serum leptin. Timepoint: Baseline and after 4 weeks. Method of measurement: ELISA assay.;BMI. Timepoint: Baseline and after 4 weeks. Method of measurement: formula.;Waist to hip ratio. Timepoint: Baseline and after 4 weeks. Method of measurement: formula.;Bady fat. Timepoint: Baseline and after 4 weeks. Method of measurement: OMRON.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamid Rasekhi

Ahvaz Jundishapur University of Medical Science

Rasekhi.h@ajums.ac.ir+98 61 1373 8253

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 18, 2026