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RecruitingNCT07245082Updated Sep 15, 2026

Patients With Type 2 Diabetes

An observational study in Diabetes Mellitus Type 2, sponsored by National Taiwan University Hospital. Recruiting at 1 site in Taiwan. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-15.

Sponsored by National Taiwan University Hospital · Observational

From the registry’s dates

  • Started Oct 2025; still recruiting 1 year 1 month later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,000
Ages
18 Years and older
Sex
All
01

Study summary

Diabetes mellitus

Read the detailed description

This study aims to establish both retrospective and prospective cohorts of patients with type 2 diabetes, enabling long-term follow-up of metabolic factors and related complications (such as cardiovascular disease, nephropathy, and neuropathy), as well as changes in nutritional status and physical function (including dietary habits, body composition, and grip strength). The goal is to identify risk factors that influence clinical outcomes and to provide evidence to support individualized treatment and integrated care strategies.

02

Conditions studied

  • Diabetes Mellitus Type 2

Keywords

  • Obesity
  • Diabetic macular edema
  • diabetic kidney disease
  • Diabetic retinopathy
  • Nutritional status
  • Physical activity
  • Peripheral Arterial Occlusive Disease
  • Body composition
  • Metabolic Syndrome
  • Dynapenia
03

In context

Diabetes Mellitus, Type 2

10,371 studies on the registry are indexed under Diabetes Mellitus, Type 2; 1,406 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 300 across 1,741 observational studies indexed under Diabetes Mellitus, Type 2.

Browse Diabetes Mellitus, Type 2 studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,615 studies on the registry; 576 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) 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

This study will recruit adult participants aged 18 years or older who have been diagnosed with type 2 diabetes mellitus (T2DM), as confirmed by medical history, diagnostic codes, or current use of hypoglycemic medications. Eligible participants must be willing to join the study and provide written informed consent. In addition, they should be able to complete the required baseline assessments, including anthropometric and functional measurements such as height, weight, waist circumference, handgrip strength, and body composition.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Adults aged 18 or older.
  2. Patients diagnosed with type 2 diabetes (based on medical history, diagnostic code, or use of hypoglycemic medication).
  3. Participants are willing to participate in the study and have signed the consent form.
  4. Participants are able to complete basic assessments (e.g., height, weight, waist circumference, grip strength, body composition, etc.).

Exclusion criteria

Exclusion Criteria:

  1. Individuals who cannot understand the study content.
  2. Individuals who cannot cooperate with relevant assessments.
  3. Other individuals who are clinically deemed unsuitable for participation by the project leader.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,000 participants (estimated)
Target follow-up
3 Years
Patient registry
Yes

Groups and cohorts

  • Cohort Study of Patients With Type 2 Diabetes
06

What researchers measure

Primary outcomes

  1. Changes in nutritional status and physical function (including dietary habits, body composition, and grip strength)

    Time frame: Everytime after physician's appointment(Usually 3 months).

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Oct 2025 (actual). Primary completion is estimated for Aug 2028, 34 months after the start.

Of 432 non-industry observational studies under Diabetes Mellitus, Type 2, half reached primary completion within 35 months of starting (the median), counting those still running; a quarter within 17 and three quarters within 96. This study's planned 34 months is close to that.

Counting every sponsor, half of 602 studies reached it within 32 months; a quarter within 17 and three quarters within 62.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 16, 2025
First posted
Nov 24, 2025
StartActual
Oct 9, 2025
Primary completionEst.
Aug 21, 2028
CompletionEst.
Aug 21, 2028
Last update
Sep 15, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07245082
Responsible party
Sponsor
First posted
Nov 24, 2025
Start date
Oct 9, 2025
Primary completion
Aug 21, 2028 (estimated)
Completion
Aug 21, 2028 (estimated)
Last update
Sep 15, 2026

Study contacts

Chia-Wen Lu, Present Professor
Contact
biopsycosocial@gmail.com
886-2-23123456 ext. 266703
Chia-Wen Lu, Present Professor
study chair · Department of Family Medicine, National Taiwan University Hospital

Oversight

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

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