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?Anti-diabetic effects of Dorema aucheri

Investigating Antihyperglycemic and Antihyperlipidemic Effects of Dorema aucheri Plant Powder in Type II Diabetic Patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014123120502N1
Enrollment
150
Registered
2015-02-23
Start date
2012-12-21
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

Patients with Type II Diabetes. Non-insulin-dependent diabetes mellitus

Interventions

Placebo group 3): receiving placebo capsules, daily before lunch + anti-diabetic medication, for 45 days
Intervention 1: Placebo group 3): receiving placebo capsules, daily before lunch + anti-diabetic medication, for 45 days. Intervention 2: Intervention group 2): receiving 500 mg capsules containing Do
Placebo
Treatment - Drugs
Intervention group 2): receiving 500 mg capsules containing Dorema aucheri (DA) powder, daily before lunch + anti-diabetic medication, for 45 days
Intervention group 1): receiving 100 mg capsules containing Dorema aucheri (DA) powder, daily before lunch + anti-diabetic medication, for 45 days

Sponsors

Shahid Sadoughi University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: a minimum of 2-year experience with type II diabetes diagnosed by a physician endocrinologist; 40-65 years of age, Exclusion criteria: free of dietary restrictions/food allergies; not receiving insulin therapy; not using medications or supplementation known to alter sugar/lipid metabolism; no clinical history of cardiovascular, hepatic, gastrointestinal, or renal disease; no recent history of smoking.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood levels of glucose. Timepoint: At the baseline of experiment and after 45 days at the end of experiment. Method of measurement: Blood testing.

Secondary

MeasureTime frame
The blood level of cholesterol. Timepoint: At the baseline of experiment and after 45 days at the end of experiment. Method of measurement: Blood testing.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Pourrajab

Shahid Sadoughi University of Medical Sciences

mina_poorrajab@yahoo.com+98 35 3820 3410

Outcome results

None listed

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