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A Research Study, Looking at the Characterization of Treatment Intensified (Add on to Metformin) Real-world Adult Population With Type 2 Diabetes Mellitus in India, Pakistan and Thailand.

A Multicentre Retrospective Study of Characterization of Treatment Intensified (Add on to Metformin) Real World Adult Population With Type 2 Diabetes Mellitus in India, Pakistan, and Thailand.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05542420
Acronym
CONVERGE
Enrollment
3000
Registered
2022-09-15
Start date
2022-10-19
Completion date
2023-04-20
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Type 2

Brief summary

This study aims to describe demographics, clinical, treatment and healthcare resource utilization characteristics with a particular focus on those relating to cardiovascular disease in selected treatment intensified patients with type 2 diabetes in the real-world settings in India, Pakistan, and Thailand. The study will be based on data already recorded in participants medical record and no new tests or procedures are required as part of the study. The study will last for about 6 months and it does not affect participants current treatment.

Interventions

OTHERNo treatment given

The study will be based on data already recorded in the medical record

Sponsors

Novo Nordisk A/S
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

1. Informed consent obtained before any study-related activities (study-related activities are any procedure related to recording of data according to the protocol). 2. Male or female, age above or equal to 18 years at type 2 diabetes mellitus (T2DM) diagnosis 3. Year of birth 1928 or later (age blow 90 years old in 2017) 4. T2DM diagnosis in medical record on or after the date of local GLP-1 RA marketing authorization 5. Medical records documenting prior or ongoing treatment with metformin 6. Medical records documenting treatment with other non-metformin T2DM drugs

Exclusion criteria

1. Previous participation in this study. Participation is defined as having given informed consent in this study. 2. Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation. 3. Patients with any diagnosis of type 1 diabetes mellitus (T1DM)

Design outcomes

Primary

MeasureTime frameDescription
The proportion of patients prescribed cardiovascular disease (CVD) medicationsSince the start of medical recordWill be reported as percent of patients
BMI (body mass index)6 months prior to Baseline (day 0, defined as the date of first prescription for the most recent antidiabetic medication drug class) (retrospective)BMI will be calculated from height and weight data reported as percent of patients
Most recent blood pressure measurement values6 months prior to Baseline (day 0, defined as the date of first prescription for the most recent antidiabetic medication drug class) (retrospective)Reported as mmHg
The proportion of patients prescribed glucagon-like peptide-1 receptor agonists (GLP-1 RA)At Baseline (day 0, defined as the date of first prescription for the most recent antidiabetic medication drug class)Will be reported as percent of patients

Countries

India, Pakistan, Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026