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Evaluation of viabet capsule, a herbal formulation, as an adjuvant treatment for diabetes mellitus type 2

Evaluation of viabet capsule, a herbal formulation, as an adjuvant treatment for diabetes mellitus type 2

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191015045124N1
Enrollment
30
Registered
2020-02-17
Start date
2020-01-07
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Type 2 diabetes. Diabetes mellitus due to underlying condition

Interventions

Intervention 1: Intervention group: viabet 500 mg three times a day for 3 months. Intervention 2: Control group: viabet placebo three times a day for 3 months.

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor
Pharmaceutical Company Essential Oil Dr Soleimani
Collaborator

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: Type 2 diabetes according to the 2019 ADA Guideline Only take metformin tablets BMI between 25 - 32

Exclusion criteria

Exclusion criteria: Pregnancy and lactation Sensitivity to drug Taking other diabetes medications except metformin taking drugs that affect blood sugar such as glucocorticoids Other serious illnesses such as heart failure Stomach or duodenal ulcer Use of anticoagulants such as heparin

Design outcomes

Primary

MeasureTime frame
Fasting blood sugar. Timepoint: Starting Study; One month later; Two months later; End of study. Method of measurement: Measurement of serum level in the laboratory.;Hemoglobin A1C. Timepoint: Starting Study; End of study. Method of measurement: Measurement of serum level in the laboratory.

Secondary

MeasureTime frame
Serum creatinine. Timepoint: starting Study; End of study. Method of measurement: Measurement of serum level in the laboratory.;Blood Urea Nitrogen. Timepoint: starting Study; End of study. Method of measurement: Measurement of serum level in the laboratory.;Aspartate aminotransferase. Timepoint: starting Study; End of study. Method of measurement: Measurement of serum level in the laboratory.;Alanine aminotransferase. Timepoint: starting Study; End of study. Method of measurement: Measurement of serum level in the laboratory.;Triglyceride. Timepoint: starting Study; End of study. Method of measurement: Measurement of serum level in the laboratory.;Cholesterol. Timepoint: starting Study; End of study. Method of measurement: Measurement of serum level in the laboratory.;Low-density lipoprotein. Timepoint: starting Study; End of study. Method of measurement: Measurement of serum level in the laboratory.;High-density lipoprotein. Timepoint: starting Study; End of study. Method of measurement: Measurement of serum level in the laboratory.;Weight. Timepoint: Starting Study; One month later; Two months later; End of study. Method of measurement: by scale.;Blood pressure. Timepoint: Starting Study; One month later; Two months later; End of study. Method of measurement: By manometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactOmid Tanzifi Roodi

Mashhad University of Medical Sciences

tasnifio9331@mums.ac.ir+98 51 3180 1588

Outcome results

None listed

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