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Therapeutic effect of chicory in type 2 diabetic patients

Evaluation of therapeutic effect of Cichorium intybus in patients with type 2 diabetes: a randomized double blind clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171220037971N1
Enrollment
90
Registered
2018-05-09
Start date
2018-05-22
Completion date
Unknown
Last updated
2018-06-18

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

Conditions

Type 2 diabetes mellitus. Type 2 diabetes mellitus

Interventions

Intervention 1: Intervention group: The intervention group in this research will receive whole chicory plant powder. Participants take 3 gr chicory powder daily as 6 capsules and take them 2 times a d

Sponsors

Bandare-abbas University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: patients with type 2 diabetes (T2DM) age from 30 to 65 years BMI less than 30kg / m ^ 2 They have been diagnosed for diabetes at least one year before entering into the study Taking anti-diabetes drugs (the type of medicine is not a criterion) not using insulin

Exclusion criteria

Exclusion criteria: Addiction to alcohol and drugs Abnormal level of liver enzymes or BUN or creatinine Any change in the type, or dosage of antidiabetic drugs or administration of insulin The presence of special diseases or condition (eg, nephropathy, thyroid disease, pregnancy, etc.) Taking medications that affect blood sugar levels Failure to follow the study protocol

Design outcomes

Primary

MeasureTime frame
Fasting blood glucose. Timepoint: investigate fasting blood glucose at the first and end of research. Method of measurement: Autoanalyzer spectrophotometer.;Hemoglobin A1c. Timepoint: investigate Hemoglobin A1c at the first and end of research. Method of measurement: Autoanalyzer spectrophotometer.;Homeostatic Model Assessment of Insulin Resistance. Timepoint: investigate Homeostatic Model Assessment of Insulin Resistance at the first and end of research. Method of measurement: Autoanalyzer spectrophotometer.

Secondary

MeasureTime frame
Serum level of triglyceride. Timepoint: investigate serum level of triglyceride at the first and end of research. Method of measurement: Autoanalyzer spectrophotometer.;Serum level of total cholesterol. Timepoint: investigate serum level of total cholesterol at the first and end of research. Method of measurement: Autoanalyzer spectrophotometer.;Serum level of low density lipoprotein cholesterol. Timepoint: investigate serum level of low density lipoprotein cholesterol at the first and end of research. Method of measurement: Autoanalyzer spectrophotometer.;Serum level of high density lipoprotein cholesterol. Timepoint: investigate serum level of high density lipoprotein cholesterol at the first and end of research. Method of measurement: Autoanalyzer spectrophotometer.;Serum level of Aspartate Aminotransferase. Timepoint: investigate serum level of Aspartate Aminotransferase at the first and end of research. Method of measurement: Autoanalyzer spectrophotometer.;Serum level of Alanine Aminotransferase. Timepoint: investigate serum level of Alanine Aminotransferase at the first and end of research. Method of measurement: Autoanalyzer spectrophotometer.;Serum level of alkaline phosphatase. Timepoint: investigate serum level of alkaline phosphatase at the first and end of research. Method of measurement: Autoanalyzer spectrophotometer.;Blood pressure. Timepoint: investigate blood pressure at the first and end of research. Method of measurement: The mercury manometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Hendijani

Bandare-abbas University of Medical Sciences

f_hendijani@pharm.mui.ac.ir+98 76 3371 0405

Outcome results

None listed

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