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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05143827
Other study ID # 15425-IGGA1
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 20, 2021
Est. completion date September 30, 2022

Study information

Verified date July 2022
Source Azienda Ospedaliero-Universitaria Careggi
Contact Edoardo Mannucci
Phone 3387861041
Email edoardo.mannucci@unifi.it
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This randomized, cross-over study compares pasta produced with three different wheat varieties (Senatore Cappelli, Korasan, Claudio). Patients with type 2 diabetes with no pharmacological treatment will be randomized to three different sequences, and asked to eat a standard portion of pasta on three different occasions, four days apart. 3-hour post-prandial interstitial glucose profiles will be recorded using trans-cutaneous sensors.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date September 30, 2022
Est. primary completion date August 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Type 2 diabetes - Body Mass Index (BMI) > 20 kg/m2 - HbA1c < 58 mmol/mol Exclusion Criteria: - Current pharmacological therapy for diabetes (of any kind) - Pregnancy or lactation

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pasta manufactured with traditional wheat varieties (Senatore Cappelli, Korasan)
A single meal composed of a portion of pasta (with standardized dressing) manufactured with different wheat varieties
Pasta manufactured with current wheat varieties (Claudio)
A single meal composed of a portion of pasta (with standardized dressing) manufactured with different wheat varieties

Locations

Country Name City State
Italy Diabetologia AOU Careggi Firenze

Sponsors (1)

Lead Sponsor Collaborator
Azienda Ospedaliero-Universitaria Careggi

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary 60-min glucose Glucose (interstitial monitoring) 60 min after beginning of meal 60 minutes
Secondary 30-min glucose Glucose (interstitial monitoring) 30 min after beginning of meal 30 minutes
Secondary 90-min glucose Glucose (interstitial monitoring) 90 min after beginning of meal 90 minutes
Secondary 120-min glucose Glucose (interstitial monitoring) 120 min after beginning of meal 120 minutes
Secondary 150-min glucose Glucose (interstitial monitoring) 150 min after beginning of meal 150 minutes
Secondary 180-min glucose Glucose (interstitial monitoring) 180 min after beginning of meal 180 minutes
Secondary Area Under the Curve (AUC) glucose 30 min Area under glucose (interstitial monitoring) curve 30 min after beginning of meal 30 minutes
Secondary AUC glucose 60 min Area under glucose (interstitial monitoring) curve 60 min after beginning of meal 60 minutes
Secondary AUC glucose 90 min Area under glucose (interstitial monitoring) curve 90 min after beginning of meal 90 minutes
Secondary AUC glucose 120 min Area under glucose (interstitial monitoring) curve 120 min after beginning of meal 120 minutes
Secondary AUC glucose 180 min Area under glucose (interstitial monitoring) curve 180 min after beginning of meal 180 minutes
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