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Crocus Sativus Extract Impact in Metabolic Control of Patients With Diabetes Mellitus Type 1

Not Applicable
Completed
Conditions
Diabetes Mellitus, Type 1
Diabetes type1
Registration Number
NCT05933460
Lead Sponsor
Aristotle University Of Thessaloniki
Brief Summary

Administration of 4 strain of probiotics, prebiotic, magnesium and crocus sativus extract in a sachet to people with diabetes mellitus type 1 for 6 months

Detailed Description

Double blind placebo controlled randomized trial: A sachet of a combination of 4 strains of probiotics (Lactobacillus rhamnosus, Bifidobacterium animalis lactis, Bifidobacterium breve, Bifidobacterium longum), Fructooligosaccharides, Magnesium and Saffron extract was administered 3 times per day in people with diabetes type 1 for 6 months on continuous glucose monitoring systems.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
61
Inclusion Criteria
  • People with diabetes mellitus type 1 (with diabetes duration over 1 year) (adults <18 years old) wearing a continuous glucose monitoring system with or without an insulin pump
Exclusion Criteria
  • Pregnant
  • People with diabetes mellitus type 2
  • Breastfeeding women
  • People with liver disease
  • People with chronic kidney disease (over stage 3)
  • People with allergy in crocus sativus
  • People that consume everyday herbs or supplements
  • People on anti platelet treatment not for prevention

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
blood glucose6 months

Fasting blood glucose (mg/dl)

serum low density lipoprotein cholesterol6 months

Low density lipoprotein cholesterol mg/dl

Diastolic Blood pressure6 months

Diastolic blood pressure mmHg

serum cholesterol6 months

Total Cholesterol mg/dl

Systolic Blood pressure6 months

Systolic blood pressure mmHg

serum High density lipoprotein cholesterol6 months

High density lipoprotein Cholesterol mg/dl

triglycerides6 months

serum Triglycerides mg/dl

glycated hemoglobin6 months

glycated hemoglobin %

Secondary Outcome Measures
NameTimeMethod
Continuous glucose monitoring data6 months

Time in range %

Continuous glucose monitoring time6 months

Time below range %

Continuous glucose monitoring time data6 months

Time above range %

Continuous glucose monitoring glycemic data6 months

Glucose Management Indicator %

Continuous glucose monitoring statistic data6 months

Coefficient of variance

Sural nerve conduction velocity6 months

Nerve conduction velocity is measured in the sural sensory nerve of both feet with Neurometrix DPNCheck

Electrochemical skin conductance6 months

Sudomotor function was assessed with SUDOSCAN, which measures electrochemical skin conductance in the feet (ESCF) and hands (ESCH)

Cardiovascular Autonomic Reflex tests6 months

Autonomic neuropathy testing included cardiovascular autonomic reflex tests (CARTs) such as heart rate variability to obtain mean circular resultant (MCR), and the 30:15 stand up test to obtain postural index and blood pressure measurement to test for orthostatic hypotension

Trial Locations

Locations (1)

University General Hospital of Thessaloniki AHEPA

🇬🇷

Thessaloníki, Central Macedonia, Greece

University General Hospital of Thessaloniki AHEPA
🇬🇷Thessaloníki, Central Macedonia, Greece

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