Electronic Titration study: e-T study
Research type
Research Study
Full title
A 16-week, randomized, open-label, parallel-group study regarding efficacy, patient reported outcomes, and safety when using a titration software medical device in comparison to standard of care titration of insulin glargine U300 in patients with type 2 diabetes
IRAS ID
213076
Contact name
Samir Purnell-Mullick
Contact email
Sponsor organisation
Sanofi-Aventis Recherche & Développement
Clinicaltrials.gov Identifier
DIAB 30767, NIHR CRN reference
Duration of Study in the UK
1 years, months, days
Research summary
The purpose of this study is to evaluate the efficacy and safety of the web tool, how patients are comfortable with the use of the web tool and how it helps patients in recommending increases or decreases of their insulin dose and thereby keeping their blood glucose level within an acceptable range. This will be compared to standard practice recommendations made by doctors.
REC name
South Central - Oxford B Research Ethics Committee
REC reference
16/SC/0695
Date of REC Opinion
26 Jan 2017
REC opinion
Further Information Favourable Opinion