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A study to assess effect of teneligliptin on heart rhythm in patients with diabetes

Phase 4
Conditions
Health Condition 1: null- Type 2 Diabetes
Registration Number
CTRI/2018/02/012072
Lead Sponsor
Torrent Pharmaceutical Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patient willing to provide informed consent

Female or male patient aged 60 years or above

Treatment naïve patients or patients who had inadequately controlled type 2 diabetes mellitus despite using diet plus exercise and/or OADs: a. HbA1C greater than 6.5% b. FBS more than or equal to 140 mg per dL

Patient is prescribed teneligliptin 40mg as a monotherapy or add on therapy

Patients must provide written consent to use personal and/or health data prior to the entry into the study

Exclusion Criteria

Patients with Type 1 diabetes mellitus

Patient on DPP-4 inhibitor other than teneligliptin and GLP-1 analogue therapy

Contraindications for teneliglitpin as per approved prescribing information

Patients taking any other drug prolonging QT interval.

Any reasons of medical and non-medical character, which in the opinion of the physician can prevent participation of subject in the study

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess the change in QTc interval in ECG from baseline to week 4 and 12Timepoint: At baseline, week 4 and week 12
Secondary Outcome Measures
NameTimeMethod
To assess the change in HbA1c, FBG and PPBG levels from baseline to week 12 <br/ ><br> <br/ ><br>To understand usage pattern of teneligliptin in diabetic patients as a monotherapy or add-on with other OADs <br/ ><br> <br/ ><br> <br/ ><br> <br/ ><br>To assess adverse events during study duration <br/ ><br>Timepoint: At baseline, week 4 and Week 12
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