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A Pilot study of anti-diabetic effects of rich Oligosaccharides fraction which is taken from Rosa arvensis in patients with type 2 diabetes

comparsion of the Effects of an anti-diabetic oligosaccharide rich fraction extracted from Rosa arvensis with common treatment on diabetic patients type2( a pilot study)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013120214333N13
Enrollment
40
Registered
2013-12-24
Start date
2013-09-23
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 of type2. Non-insulin dependent diabetes mellitus

Interventions

Intervention 1: The intervention group receive three capsules daily, each containing 350 mg of rich Oligosaccharides fraction taken from Rosa arvensis which is added to the standard treatment and in c
Treatment - Drugs
The intervention group receive three capsules daily, each containing 350 mg of rich Oligosaccharides fraction taken from Rosa arvensis which is added to the standard treatment and in case of decreasin
Control group receive treatment with a common protocol.

Sponsors

Barekat Pharmaceutical Company
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: diabetes diagnosis with fasting blood sugar over 125, or postprandial glucose over 200 or glycosylated hemoglobin level greater than 6; patient willingness and signed informed consent, age less than 65 years; history of diabetes less than 10 years; diabetes onset at least three months before. Exclusion criteria: requiring insulin injections or diagnosis of type 1 diabetes, kidney disease, liver disease, cancer, anemia and heart failure, pregnancy, glycosylated hemoglobin over 10, corticosteroids use.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood sugar (FBS). Timepoint: Baseline, 3 and 6 months after starting the study. Method of measurement: Test.;Glucose tolerance test (BS). Timepoint: Baseline, 3 and 6 months after starting the study. Method of measurement: Test.;Hba1c rate. Timepoint: Baseline, 3 and 6 months after starting the study. Method of measurement: Test.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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