Skip to content

Study on effects of sage in treatment of hypercholesterolemic type 2 diabetic patients

Study on effects of Salvia officinalis L. leaf extract in treatment of hypercholesterolemic type 2 diabetic patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201506082288N7
Enrollment
60
Registered
2015-06-28
Start date
2012-04-20
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: Sage leaf extract at the dose of one 500 mg capsule every 8 hours besides synthetic anti-hyperglycemic and anti-hyperlipidemic drugs are administered to a group of about 30 patients fo
Treatment - Drugs
Placebo
Sage leaf extract at the dose of one 500 mg capsule every 8 hours besides synthetic anti-hyperglycemic and anti-hyperlipidemic drugs are administered to a group of about 30 patients for 2 months.
One placebo capsule every 8 hours besides synthetic anti-hyperglycemic and anti-hyperlipidemic drugs are administered to a group of about 30 patients for 2 months.

Sponsors

Iranian Academic Center for Education, Culture and Research Institute of Medicinal Plants
Lead Sponsor
Tehran University of Medical Sciences Diabetes Research Center
Collaborator

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Iranian male and female type 2 diabetic outpatients; patients aged 40 to 60 years; patients with blood HbA1c levels below 8%; patients with serum LDL levels from 100 mg/dl to 130 mg/dl; patients receiving standard therapy with synthetic anti-hyperglycemic and anti-hyperlipidemic drugs. Exclusion criteria: Patients receiving insulin; patients with cardiac, renal, hepatic, hematological diseases, hypothyroidism, tachycardia, vertigo and seizure; patients with a history of gallstones or gall bladder surgery; patients using estrogen, steroid, beta-blocker and thiazide; pregnant women; women planning pregnancy; breast-feeding women.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fasting serum glucose level. Timepoint: 2 months. Method of measurement: Medical laboratory (kit).;Glycosylated hemoglobin blood level. Timepoint: 2 months. Method of measurement: Medical laboratory (kit).;LDL serum level. Timepoint: 2 months. Method of measurement: Medical laboratory (kit).

Secondary

MeasureTime frame
Serum triglyceride level. Timepoint: 2 months. Method of measurement: Medical laboratory (kit).;Serum total cholesterol level. Timepoint: 2 months. Method of measurement: Medical laboratory (kit).;Serum creatinine level. Timepoint: 2 months. Method of measurement: Medical laboratory (kit).;Serum 2 hour postprandial glucose level. Timepoint: 2 months. Method of measurement: Medical laboratory (kit).;Serum SGOT level. Timepoint: 2 months. Method of measurement: Medical laboratory (kit).;Serum SGPT level. Timepoint: 2 months. Method of measurement: Medical laboratory (kit).;Serum HDL level. Timepoint: 2 months. Method of measurement: Medical laboratory (kit).;Body mass index. Timepoint: 2 months. Method of measurement: Weighing scales and tape.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Saeed Kianbakht

Iranian Academic Center for Education, Culture and Research Institute of Medicinal Plants

skianbakht@yahoo.comskianbakht@gmail.com+98 26 3476 4010

Outcome results

None listed

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