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The effect of saffron tablet in obese prediabetic patients

The effect of saffron tablet on lipid profiles and blood glucose and oxidative stress in obese prediabetic patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120913010826N19
Enrollment
80
Registered
2018-01-04
Start date
2017-11-01
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

Obese Pre-dabetic. Impaired glucose tolerance (oral)

Interventions

Intervention 1: The control group will receive placebo (the same as saffron pill in doses of 15mg)once a day for 8 weeks. Intervention 2: The intervention group will receive saffron pill in dosage 15
Placebo
Treatment - Drugs
The control group will receive placebo (the same as saffron pill in doses of 15mg)once a day for 8 weeks
The intervention group will receive saffron pill in dosage 15 mg ,once a day (for 8 weeks)

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: all patients which are defined as pre-diabetes who referring to the Imam Ali nutrition clinic all patients with BMI greater than 25 who referring to the Imam Ali nutrition clinic

Exclusion criteria

Exclusion criteria: Pregnancy change in diet or physical activity change in dosage change in type of drug Lack of interest in cooperation having other diseases in during the study Do not use more than 30% pills

Design outcomes

Primary

MeasureTime frame
LDL (lipid profile index). Timepoint: Before and after intervention. Method of measurement: Standards of medical diagnostic laboratories.;TG (lipid profile index). Timepoint: Before and after intervention. Method of measurement: Standards of medical diagnostic laboratories.;Cholesterol(lipid profile index). Timepoint: Before and after intervention. Method of measurement: Standards of medical diagnostic laboratories.

Secondary

MeasureTime frame
Triglyceride, , LDL-Chol, BUN, Creatinine, DPPH. Timepoint: before and after intervention. Method of measurement: Standards of medical diagnostic laboratories.;Cholesterol. Timepoint: before and after intervention. Method of measurement: Standards of medical diagnostic laboratories.;LDL cholesterol concentration. Timepoint: before and after intervention. Method of measurement: Standards of medical diagnostic laboratories.;BUN. Timepoint: before and after intervention. Method of measurement: Standards of medical diagnostic laboratories.;Creatinine. Timepoint: before and after intervention. Method of measurement: Standards of medical diagnostic laboratories.;DPPH. Timepoint: before and after intervention. Method of measurement: Standards of medical diagnostic laboratories.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Azadeh Nadjarzadeh

shahid sadoughi university of medical sciences

azadnajarzadeh@ssu.ac.ir+98 35 3149 2239

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 2, 2026