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CompletedNCT06592950DCEUpdated Sep 19, 2024

Patient Preference Study in Type-2 Diabetes Mellitus: Discrete Choice Experiment (DCE) to Support Novo Nordisk's Long-Acting Insulin

An observational study in Type-2 Diabetes Mellitus (T2DM), sponsored by Novo Nordisk A/S. Completed at 1 site in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-09-19.

Sponsored by Novo Nordisk A/S · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
513
Ages
18 Years and older
Sex
All
01

Study summary

The primary objective of this research is to assess T2DM patient preferences for a once weekly insulin treatment. The study involves a qualitative interview phase and quantitative survey phase with a Discrete Choice Experiment (DCE).

02

Conditions studied

  • Type-2 Diabetes Mellitus (T2DM)
03

In context

Diabetes Mellitus

10,925 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's enrollment of 513 is above the median of 233 across 2,220 observational studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

Novo Nordisk A/S is the lead sponsor of 1,370 studies on the registry; 102 are open to participants now.

Of its 198 completed or terminated interventional studies of FDA-regulated products, 94 (47%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Type-2 diabetes mellitus (T2DM) patients

Inclusion criteria

  • Patient is an adult aged 18 years or over
  • Patient was diagnosed with type-2 diabetes mellitus (T2DM) greater than or equal to 180 days prior to the day of screening
  • Patient is currently prescribed a diabetes treatment (e.g., Metformin/Sus, DPP4i, SGLT2i, GLP-1 RA and/or basal insulin)
  • Patient is willing and able to provide written informed consent to participate

For qualitative interviews:

  • Patient is a fluent speaker of English and is able to read, write, and fully understand the English language
  • Patient is a resident in Canada

For quantitative online survey:

  • Patient is a fluent speaker of the local language (English/French/Spanish or Japanese) and is able to read, write and fully understand the local language
  • Patient is a resident of either Canada, France, Spain or Japan

Exclusion criteria

Exclusion Criteria:

  • Patient is currently employing a basal-bolus insulin treatment regimen to manage their diabetes
  • Patient is unwilling or unable to comply with the needs of the study or has a physical, behavioural or mental condition that, in the opinion of the recruiter may affect the patient's ability to take part in the study, understand the nature, scope and possible consequences of the study, or the responses they might provide.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
513 participants (actual)
Patient registry
No

Groups and cohorts

  • Quantitative online survey

    Across four markets (Canada, France, Spain and Japan)

    Other: No treatment given

  • Qualitative interviews

    Conducted in Canada

    Other: No treatment given

Interventions

  • OtherNo treatment given

    Online survey

  • OtherNo treatment given

    Interviews

06

What researchers measure

Primary outcomes

  1. T2DM patient preferences for a once weekly insulin treatment

    Pre-defined open-ended questions and Discrete Choice Experiment online survey

    Time frame: Day of interview/survey completion (Day 1)

07

Study locations

1 site
  • Novo Nordisk
    Søborg, 2860, Denmark
08

References and documents

Individual participant data

Plan to share: Yes — According to the Novo Nordisk disclosure commitment on novonordisk-trials.com

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 19, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06592950
Lead sponsor
Novo Nordisk A/S
Responsible party
Sponsor
First posted
Sep 19, 2024
Start date
Nov 2, 2023
Primary completion
Apr 29, 2024
Completion
Apr 29, 2024
Last update
Sep 19, 2024

Study contacts

Clinical Transparency dept. 2834
study director · Novo Nordisk A/S

Oversight

Data monitoring committee
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2024. You cannot join it, but the record below documents what was studied.

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