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Clinical Trials/CTRI/2017/10/010218
CTRI/2017/10/010218
Active, not recruiting
Phase 4

A multi-centre prospective, non-interventional study of ability and willingness to pay for BIAsp 30 in a real world population with type 2 diabetes mellitus - NA

ovo Nordisk India Private Ltd0 sites0 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
ovo Nordisk India Private Ltd
Status
Active, not recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational

Investigators

Sponsor
ovo Nordisk India Private Ltd

Eligibility Criteria

Inclusion Criteria

  • 1\. The decision to initiate treatment with commercially available BIAsp 30 has been made by the patient and the treating physician before and independently from the decision to include the patient in this study.
  • 2\. Patients selected by their physician for participation in the study, who are likely to be able and willing to pay for the BIAsp 30 treatment for at least 12 weeks from baseline visit as assessed by the treating physician.
  • 3\. Signed informed consent obtained before any study\-related activities (study\-related activities are any procedure related to recording of data according to the protocol).
  • 4\. Male or female more than or equal to 18 years at time of informed consent.
  • 5\. Diagnosed with T2DM and treated with BHI in vials for at least three consecutive months at time of informed consent.

Exclusion Criteria

  • 1\. Previous participation in this study. Participation is defined as having given informed consent in this study.
  • 2\. Concurrent participation in any other clinical trial or study.
  • 3\. Patients previously treated with insulin analogues.
  • 4\. Known or suspected hypersensitivity to study product (or any of the excipients of the study product; a full list of excipients is provided in Summary of product characteristics (SmPC) of NovoMix® 3011\) or related products.
  • 5\. Mental incapacity, unwillingness, or language barriers precluding adequate understanding or cooperation.
  • 6\. Patients who are unable to read or write (illiterate).

Outcomes

Primary Outcomes

Not specified

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