Skip to content

A single-center, single-arm efficacy study evaluating the effects of alogliptin on HbA1c levels and blood glucose control in patients with type 2 diabetes mellitus (T2DM) experiencing relapse after 12 weeks of treatment

A single-center, single-arm efficacy study evaluating the effects of alogliptin on HbA1c levels and blood glucose control in patients with type 2 diabetes mellitus (T2DM) experiencing relapse after 12 weeks of treatment

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103072
Enrollment
Unknown
Registered
2025-05-23
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Type 2 diabetes mellitus

Interventions

Coagliptin group:Treated with codagliptin

Sponsors

Tongji Hospital, Tongji Medical College ,Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Can understand and voluntarily sign the written informed consent form; 2.Age >=18 years old; 3.Patients met the criteria for recurrence after remission of type 2 diabetes mellitus, i.e., glycosylated hemoglobin (HbA1c) could not be maintained <6.5% after stopping glucose-lowering drugs for at least 3 months; and HbA1c<8.5%; 4.Coogliptin monotherapy was required, as judged by the investigator;

Exclusion criteria

Exclusion criteria: 1.Participated in any other clinical study within 30 days before screening; 2.Patients with severe organ dysfunction or malignant tumor of the heart, liver, kidney, etc; 3.Pregnant or lactating women; 4.Allergy to coagliptin or other drug components used in this study; 5.Persons with severe mental illness or cognitive impairment; 6.There were other conditions deemed by the investigator to be inappropriate for participation in the study;

Design outcomes

Primary

MeasureTime frame
Glycated hemoglobin;

Secondary

MeasureTime frame
Two hours postprandial blood glucose;Fasting blood glucose;Blood insulin;Fasting C-peptide;Adverse events during the treatment period;Two hours postprandial C-peptide;

Countries

China

Contacts

Public ContactShao Shiying

Tongji Hospital, Tongji Medical College ,Huazhong University of Science and Technology

shaoshiyingtj@163.com+86 13627144576

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026