Classification of Adult-onset Diabetes in Five Subgroups in Pakistani Population

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age16+
SponsorGetz Pharma

About this trial

This study aims to classify adult-onset diabetes patients into distinct data-driven clusters, such as severe insulin-deficient, severe insulin-resistant, mild obesity-related, and mild age-related diabetes, based on clinical and biochemical characteristics. Using a cross-sectional design, data will be collected from individuals attending outpatient diabetes clinics at tertiary care hospitals in Pakistan. The study will analyze the distribution of metabolic and demographic characteristics within each cluster and assess subgroup-specific risks for diabetic complications. Additionally, the relationship between clustering variables and the risk of complications will be evaluated to enhance the understanding of diabetes heterogeneity and its impact on patient outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients of both genders whose age of disease onset was older than 16 years

Patients newly diagnosed with or previously diagnosed with T2D

Able and willing to provide written informed consent and to comply with the study

Disqualifiers

Patients with other medical comorbidities (not a complication of diabetes), such as malignancies.

Pregnancy

Trial population

The study population will consist of adult patients diagnosed with diabetes who are receiving care at endocrinology clinics across Pakistan. Participants will be recruited from outpatient diabetes clinics during their routine visits. The population represents a diverse group of individuals from various socioeconomic and demographic backgrounds, reflecting the heterogeneity of diabetes presentation in the region

Trial design

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Classify patients into data-driven clusters (e.g., severe insulin-deficient, severe insulin-resistant, mild obesity-related and mild age-related diabetes).

Time frame
At the time of clinic visit during enrollment

Secondary outcomes

1

Analyze the distribution of metabolic and demographic characteristics within each cluster.

Time frame
At the time of clinic visit during enrollment
2

• Assess subgroup-specific risks for diabetic macrovascular complications such as CVD, Stroke/TIA, and microvascular complications such as nephropathy, retinopathy, peripheral and autonomic neuropathy

Time frame
At the time of clinic visit during enrollment
3

Evaluate the relationship between clustering variables and complications.

Time frame
At the time of clinic visit during enrollment

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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