Type 2 Diabetes Clinical Trial
— AGO01Official title:
Efficacy, Safety and Satisfaction of the New Pen Needle 33G x 4 mm 33G x 4 mm: Cross-over Randomized Controlled Clinical Trial. Studio AGO 01
Verified date | March 2014 |
Source | Consorzio Mario Negri Sud |
Contact | n/a |
Is FDA regulated | No |
Health authority | Italy: Ministry of Health |
Study type | Interventional |
During the last years, even more little needles are used for the injection of sub cutaneous
insulin, for the diabetes therapy.
The aim of this study is to evaluate the non inferiority of a new needle, smaller than
another needle, in terms of hematic levels od fructosamine, an indicator of glycemic
control.
Status | Completed |
Enrollment | 87 |
Est. completion date | November 2013 |
Est. primary completion date | September 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - patients with type 1 or type 2 diabetes - both males and females - age >=18 anni - insulin treatment from at least 6 months - signed informed consent Exclusion Criteria: - pregnancy - incapacity for filling in the questionnaires - every illness or condition that, according to the investigator, could interfere with the study |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Italy | UO Diabetologia per Trattamento e Educazione dei Diabetici - Spedali Civili di Brescia | Brescia | BS |
Italy | U.O.S. Diabetologia e Malattie Metaboliche - PO Cantù - Mariano Comense | Mariano Comense | CO |
Italy | Struttura Complessa Dietologia-Diabetologia Malattie Metaboliche - Ospedale Pertini | Roma | RM |
Italy | UO Malattie Metaboliche e Diabetologia - Ospedale di Treviglio-Caravaggio | Treviglio | BG |
Lead Sponsor | Collaborator |
---|---|
Consorzio Mario Negri Sud | Artsana SpA |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | hematic fructosamine levels | Change from baseline in fructosamine levels after 3 weeks of treatment | No | |
Secondary | mean amplitude of glucose excursions (MAGE) | Change from baseline in MAGE after 3 weeks of treatment | No | |
Secondary | pain | visual analogic scale (VAS) 1-10 | questionnaire at the end of the treatments (at 6 weeks) | No |
Secondary | leakage at the site injection | visual scale | number of episodes of leakage during the treatment (3 weeks) | No |
Secondary | hypoglycemia | number of episodes of hypoglycemia during the treatment (3 weeks) | Yes | |
Secondary | insulin dosage | Change from baseline in insulin dosage after 3 weeks of treatment | No | |
Secondary | patient's weight | Change from baseline in weight after 3 weeks of treatment | No | |
Secondary | patient's satisfaction | VAS scale | questionnaire at the end of the treatments (at 6 weeks) | No |
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