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Effects of Diabetan and Saliva officinalis L tablets on blood glucose levels of patients with type 2 DM.

Effects of Diabetan and Saliva officinalis L tablets on blood glucose levels of patients with type 2 DM.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201011112696N2
Enrollment
80
Registered
2010-12-18
Start date
2010-10-23
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 Melitus (DM). Diabetes Melitus

Interventions

Intervention 1: Diabetan tablet will be prescribed for them 3 times per day for three months. Intervention 2: Placebo tablet will be prescribed 3 times per day for three months.
Treatment - Drugs
Placebo
Diabetan tablet will be prescribed for them 3 times per day for three months
Placebo tablet will be prescribed 3 times per day for three months.

Sponsors

Gol Daru Co.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 149 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1-Having type 2 diabetes based on internal criteria with FBS=126 or more and blood glucose 200 or more in daytime. 2- HbA1C more than 7% and less than 9% 3-Not having side effects of DM 4-Non- insulin dependent 5-Willing to participate in the trial 6-Not having a crucial illness 7- psychologically normal 8- Not using any other drugs for other diseases. Excluding Criteria: 1- Hyperglycemia with HbA1C more than 250 2-2hpp more than 9% and less than 7% 3-Pragnancy and lactation 4- Using insulin 5- Not willing to enter the trial 6- Having side effects of DM 7- Cardiovascular, hepatic, renal and other major systemic diseases 8- psychologically abnormal 9- Using drugs for other illnesses 10- Type 1 DM 11- Age less than 30 years

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
HbA1C. Timepoint: At the beginning and at the end of trial (in 3 months. Method of measurement: Laboratory mg/ dl.;Lipid profile. Timepoint: At the beginning and end of the trial (in 3 months). Method of measurement: mg/dl through lab methods.;Liver and kidney parameters. Timepoint: At the beginning and end of the trial (in 3 months). Method of measurement: mg/dl through lab methods.;FBS and HbA1C. Timepoint: at the beginning of trial and every 2 weeks. Method of measurement: mg/dl.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohamad Saeed Behradmanesh

Shahrekord University of Medical Sciences

behradmanesh@skums.ac.ir+98 38 1333 0709

Outcome results

None listed

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