Actively Recruiting
A Study to Identify and Characterize Patients With Type 2 Diabetes Mellitus for Possible Participation in Ongoing or Future Type 2 Diabetes Mellitus Clinical Studies
Led by AstraZeneca · Updated on 2026-05-26
3000
Participants Needed
40
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying patients with Type 2 Diabetes Mellitus (T2DM) to identify and describe their characteristics for possible involvement in current or future clinical trials focused on T2DM. The study aims to understand medication use patterns among these patients across different regions and better characterize their health status. Participants include adults with T2DM who are managed either through lifestyle changes alone or with stable doses of glucose-lowering medicines. The study involves a one-time visit during which participants will undergo assessments including blood collection (about 2 mL) and evaluation of their medical history, demographics, medication use, and blood sugar levels measured by HbA1c. During the single visit, researchers will collect information about medical and surgical history, current medications, and demographic data. They will measure HbA1c levels to assess blood sugar control and may refer participants to other ongoing or future T2DM studies. The study focuses on observation and data collection without active treatment, lasting only one day for each participant.
CONDITIONS
Brief Title
A Study to Identify and Characterize Patients With Type 2 Diabetes Mellitus for Possible Participation in Ongoing or Future Type 2 Diabetes Mellitus Clinical Studies
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants must be 18 years of age or older at the time of signing the informed consent form.
- Diagnosed with Type 2 Diabetes Mellitus confirmed by testing or medical records according to WHO or local standards.
- Diabetes is managed either by lifestyle changes alone or with a stable dose of glucose-lowering medication(s) for at least 45 days before consenting.
- Interested and willing to participate in ongoing or future Type 2 Diabetes clinical studies and able to follow study procedures.
- Provide signed and dated informed consent before any study procedures or tests.
You will not qualify if you...
- Current or planned use of GLP-1 receptor agonists that are prohibited in ongoing or future investigational studies.
- Diagnosis of Type 1 diabetes mellitus.
- Known pregnancy or intention to become pregnant at the time of the visit.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo assessments including blood sampling and medical history review.
1 visit (in-person)
Trial Site Locations
Total: 40 locations
1
Research Site
Lincoln, California, United States, 95648
Actively Recruiting
2
Research Site
Ocoee, Florida, United States, 34761
Not Yet Recruiting
3
Research Site
Decatur, Georgia, United States, 30030
Not Yet Recruiting
4
Research Site
Potomac, Maryland, United States, 20854
Not Yet Recruiting
5
Research Site
Gaffney, South Carolina, United States, 29340
Not Yet Recruiting
6
Research Site
Renton, Washington, United States, 98057
Not Yet Recruiting
7
Research Site
Fortaleza, Ceará, Brazil, 60430-350
Not Yet Recruiting
8
Research Site
Curitiba, Paraná, Brazil, 80030-480
Not Yet Recruiting
9
Research Site
Natal, Rio Grande do Norte, Brazil, 59020-035
Not Yet Recruiting
10
Research Site
Porto Alegre, Rio Grande do Sul, Brazil, 90630-165
Not Yet Recruiting
11
Research Site
Campinas, São Paulo, Brazil, 13060-904
Not Yet Recruiting
12
Research Site
São José dos Campos, São Paulo, Brazil, 12243-280
Not Yet Recruiting
13
Research Site
São Paulo, São Paulo, Brazil, 01228-200
Not Yet Recruiting
14
Research Site
São Paulo, São Paulo, Brazil, 04012-180
Not Yet Recruiting
15
Research Site
Barretos, Brazil, 14784-400
Not Yet Recruiting
16
Research Site
Brasília, Brazil, 71625-009
Not Yet Recruiting
17
Research Site
Rio de Janeiro, Brazil, 22270-060
Not Yet Recruiting
18
Research Site
Tianjin, China, 300457
Not Yet Recruiting
19
Research Site
Seremban, Negeri Sembilan, Malaysia, 70300
Not Yet Recruiting
20
Research Site
Seri Manjung, Perak, Malaysia, 32040
Not Yet Recruiting
21
Research Site
Batu Caves, Selangor, Malaysia, 68100
Not Yet Recruiting
22
Research Site
Kuala Lumpur, Wilayah Persekutuan Kuala Lump, Malaysia, 59100
Not Yet Recruiting
23
Research Site
Putrajaya, Malaysia, 62250
Not Yet Recruiting
24
Research Site
Lublin, Lublin Voivodeship, Poland, 20-718
Not Yet Recruiting
25
Research Site
Krakow, Malopolska, Poland, 31-261
Not Yet Recruiting
26
Research Site
Radom, Masovian Voivodeship, Poland, 26-600
Not Yet Recruiting
27
Research Site
Bialystok, Podlaskie Voivodeship, Poland, 15-879
Not Yet Recruiting
28
Research Site
Częstochowa, Silesian Voivodeship, Poland, 42-217
Not Yet Recruiting
29
Research Site
Poznan, Poland, 60-354
Not Yet Recruiting
30
Research Site
Warsaw, Poland, 00-124
Not Yet Recruiting
31
Research Site
Lodz, Łódź Voivodeship, Poland, 90-338
Not Yet Recruiting
32
Research Site
Kielce, Świętokrzyskie Voivodeship, Poland, 25-355
Not Yet Recruiting
33
Research Site
Yüreğir, Adana, Turkey (Türkiye), 1240
Not Yet Recruiting
34
Research Site
Ankara, Turkey, Turkey (Türkiye), 6100
Not Yet Recruiting
35
Research Site
Adana, Turkey (Türkiye), 1060
Not Yet Recruiting
36
Research Site
Ankara, Turkey (Türkiye), 6530
Not Yet Recruiting
37
Research Site
Gaziantep, Turkey (Türkiye), 27470
Not Yet Recruiting
38
Research Site
Istanbul, Turkey (Türkiye), 34300
Not Yet Recruiting
39
Research Site
Istanbul, Turkey (Türkiye), 34384
Not Yet Recruiting
40
Research Site
Kayseri, Turkey (Türkiye), 38039
Not Yet Recruiting
Research Team
A
AstraZeneca Clinical Study Information Center
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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