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The effect of herbal supplement in type 2 diabetes treatment.

Evaluation of the effectiveness of a new herbal formulation for improving blood sugar control in patients with type 2 diabetes mellitus.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201109207602N1
Enrollment
60
Registered
2015-01-06
Start date
2014-12-22
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. Diabetes mellitus

Interventions

Intervention 1: The placebo will be prescribed one tablet orally per day to the control group for two months. Intervention 2: The herbal formulation will be prescribed one tablet orally per day to the
Treatment - Drugs
The placebo will be prescribed one tablet orally per day to the control group for two months.
The herbal formulation will be prescribed one tablet orally per day to the intervention group for two months.

Sponsors

Iran's National Elites Foundation (INEF)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:newly diagnosed diabetes according to ADA 2014 (FPG=>126 mg/dl or HgA1C=>6.4% or BS=>200 mg/dl after OGTT or random BS =>200 and hyperglycemic symptoms); age 30-65 years; signed consent form. Exclusion criteria: Diabetes type 1; insulin injection during 8 weeks ago; serious infectious diseases; renal failure (GFR< 50 cc/min/); liver failure ( high ALTor/and AST more than 3 times above normal range); cardiac failure; pregnancy and/or breast feeding; past history of seizure or epilepsy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood Glucose. Timepoint: In the beginning and at the end of 4th and 8th weeks of the trial. Method of measurement: Blood test.

Secondary

MeasureTime frame
Blood insulin. Timepoint: In the beginning and at the end of 4th and 8th weeks of the trial. Method of measurement: Blood test.;Cholesterol and triglyceride. Timepoint: In the beginning and at the end of 8th week of the trial. Method of measurement: Blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Sarkhail

Pharmaceutical Sciences Research Center

sarkhail@sina.tums.ac.ir+98 21 6412 2326

Outcome results

None listed

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