Insulin Administration Plus a Telemedicine System (Diabetes Interactive Diary - DID) vs Insulin Plus Common Practice
NCT ID: NCT01192711
Last Updated: 2010-09-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE3
130 participants
INTERVENTIONAL
2009-05-31
Brief Summary
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Aim of the study is to compare an insulin regimen of insulin glargine + prandial insulin glulisine associated with a telemedicine system to teach CHO counting (DID) with the same insulin regimen administered according to usual practice.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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insulin + DID
Three prandial (before or at the end of meal administration, based on doctor counselling and patient decision) injections per day of insulin glulisine associated with basal insulin glargine; the DID will be used to estimate the CHO content of the food intended to eat. Insulin doses in this group will be adjusted based on DID calculations and pre-meal BG values.
Diabetes Interactive Diary (DID)
DID is both a CHO/insulin bolus calculator, an information technology and a telemedicine system based on the communication between health care professional (physician or dietitian) and patient by SMS messages.
insulin + usual care
Three prandial (before or at the end of meal administration, based on doctor counselling and patient decision) injections of insulin glulisine associated with basal insulin glargine. Insulin doses in group B will be adjusted based on SMBG values reviewed during the doctor office visit.
No interventions assigned to this group
Interventions
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Diabetes Interactive Diary (DID)
DID is both a CHO/insulin bolus calculator, an information technology and a telemedicine system based on the communication between health care professional (physician or dietitian) and patient by SMS messages.
Eligibility Criteria
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Inclusion Criteria
* Males and females
* Age equal or more than 18 years
* Patients not habitually using CHO (carbohydrates) counting
* Self monitoring blood glucose (SMBG) at least 3 times a day
* Four basal-bolus daily injections of short-acting and long-acting insulin analogues
* HbA1c equal or more than 7.5%
* Female patients have to be postmenopausal, hysterectomised or surgically sterilized or using reliable and adequate contraceptive methods (oral contraception or IUD);
* A full study-specific informed consent must be obtained in writing for all subjects
Exclusion Criteria
* Mental conditions, depression, or high anxiety rendering the subject unable to understand the nature, scope, and possible consequences of the study
* Eating disorders
* Pregnancy / lactation.
* Any clinically significant major organ system disease such as relevant cardiovascular, gastrointestinal, hepatic, neurological, endocrine, haematological or other major systemic diseases or infective diseases making implementation of the protocol or interpretation of the study results difficult
* Any disease or condition including abuse of illicit drugs, prescription medicines or alcohol that in the opinion of the investigator may interfere with the completion of the study
* Subjects unlikely to comply with protocol, e.g., uncooperative attitude, inability to return for follow-up visits, and unlikelihood of completing the study procedures.
18 Years
ALL
No
Sponsors
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Sanofi
INDUSTRY
LifeScan
INDUSTRY
Consorzio Mario Negri Sud
OTHER
Responsible Party
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Consorzio Mario Negri Sud
Principal Investigators
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Antonio Nicolucci, MD
Role: STUDY_CHAIR
Consorzio Mario Negri Sud
Locations
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Ospedale G.B. Morgagni - L. Pierantoni
Forlì, , Italy
P.O. di Grosseto - Stabilimento Misericordia
Grosseto, , Italy
Az. Osp. S. Anna - Presidio Ospedaliero Cantù - Mariano Comense
Mariano Comense, , Italy
Istituto Scientifico San Raffaele
Milan, , Italy
Ospedale Niguarda Cà Granda
Milan, , Italy
II Università di Napoli Centro Regionale di Diabetologia Pediatrica "G. Stoppoloni"
Naples, , Italy
Università degli Studi di Padova Dipartimento di Medicina Clinica e Sperimentale
Padua, , Italy
Ospedale Cisanello
Pisa, , Italy
U.O. di Diabetologia, Dip. di Malattie Digestive & Metaboliche
Ravenna, , Italy
Ospedale Infermi
Rimini, , Italy
Ospedale Sandro Pertini
Rome, , Italy
Ospedale Magati
Scandiano, , Italy
Azienda Ospedaliera-Universitaria S. Giovanni Battista
Turin, , Italy
Countries
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Central Contacts
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Facility Contacts
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Related Links
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Related Info
Other Identifiers
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MTD003
Identifier Type: -
Identifier Source: org_study_id
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