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Effect of Boswellia serrata on diabetes

Effect of Boswellia serrata on blood glucose, insulin, fasting insulin resistance index, fructose amine and lipid profile in type (II) diabetes patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201112258515N1
Enrollment
30
Registered
2013-10-18
Start date
2012-01-21
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

type (II) diabetes patients. Insulin-dependent diabetes mellitus, Non-insulin-dependent diabetes mellitus, Malnutrition-related diabetes mellitus, Other specified diabetes mellitus, Unspecified diabetes mellitus

Interventions

Intervention 1: Test group received oral hypoglycemic agents and Boswellia serrata for 4 weeks (300 mg, three times, chewing and package form) administrated daily. blood samples before and after 4 wee
Treatment - Drugs
Test group received oral hypoglycemic agents and Boswellia serrata for 4 weeks (300 mg, three times, chewing and package form) administrated daily. blood samples before and after 4 weeks of it being d
control group randomized selected from Type 2 diabetic patients during trial,has been treated only with oral hypoglycaemic agents. blood samples before and after 4 weeks of it being done.

Sponsors

Vice Chancellor for Research, Ahvaz Jundishapur University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Including criteria to study: age range between 30-65 years; only use the oral hypoglycemic agents; type 2 diabetic patients Exclusion criteria to study: have Hepatic cirrhosis; pregnant and lactating women; active Proliferative Diabetic Retinopathy (PDR); Chronic Kidney Disease (CKD); Congestive Heart

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood glucose. Timepoint: before and 45 days after intervention. Method of measurement: glucose kit.

Secondary

MeasureTime frame
Insulin. Timepoint: before and 45 days after intervention. Method of measurement: insulin kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAkram Ahangarpour

61335189, Department of Physiology, Diabetes Research Center and Physiology Research Center, Ahvaz J

akramahangarpour@gmail.com+98 916 608 0817

Outcome results

None listed

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