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The effect of hydro alcoholic extract of Juglans regia leaves on blood glucose in adults with type 2 diabetes

The effect of hydro alcoholic extract of Juglans regia leaves on blood glucose in adults with type 2 diabetes

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138901203180N2
Enrollment
40
Registered
2010-06-06
Start date
2010-05-01
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

Diabetes mellitus. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: Intervention group: capsule contains 100 mg of hydro alcoholic extract of Juglans regia leaves, twice daily for 8 weeks. Intervention 2: Placebo group: flour of bean capsul, twice dail
Treatment - Drugs
Placebo
Intervention group: capsule contains 100 mg of hydro alcoholic extract of Juglans regia leaves, twice daily for 8 weeks

Sponsors

Mazandaran University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 30 to 80, HbA1C>7% in spite of using 50% of maximal dose of two antidiabetic drug. Exclusions criteria: Immune deficiency, pregnancy and lactation, cardiovascular disease, currently receiving corticosteroids and thiazide, uncontrolled thyroid dysfunction, acute infection ,history of diabetic ketoacidosis , Cr>1.5 for male, Cr>1.2 for female, acute hepatitis, cirrhosis, proliferative retinopathy and severe weight loss (at least 10% during last 6 months)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
HbA1C. Timepoint: before and after intervention. Method of measurement: laboratory.;FBS. Timepoint: before and 4 and 8 weeks after intervention. Method of measurement: laboratory.

Secondary

MeasureTime frame
Serum insulin. Timepoint: before and 8 weeks after intervention. Method of measurement: laboratory.;Lipid profile. Timepoint: before and 4 and 8 weeks after intervention. Method of measurement: laboratory.;Weight. Timepoint: before and after intervention. Method of measurement: weight Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Rabie

Mazandaran University of Medical Sciences and Health Services

mprabie@yahoo.com+98 15 1226 1701

Outcome results

None listed

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