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Parallel controlled clinical study of umbilical cord mesenchymal stem cells in treatment of adult latent immune diabetes mellitus (LADA)

Parallel controlled clinical study of umbilical cord mesenchymal stem cells in treatment of adult latent immune diabetes mellitus (LADA)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047597
Enrollment
Unknown
Registered
2021-06-20
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

latent autoimmune diabetes in adults

Interventions

Sponsors

Shandong Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 60 years; 2. The diagnosis of latent immune diabetes (LADA) was established (according to the 2012 consensus on diagnosis and treatment of latent autoimmune diabetes in adults (LADA)); 3. Islet autoantibodies are positive, and GAD is the first recommended antibody to be detected; 4. Do not rely on insulin therapy for at least six months after the diagnosis of diabetes.

Exclusion criteria

Exclusion criteria: 1. Those who are pregnant, breastfeeding or intend to become pregnant, women of childbearing age who do not use effective contraceptive measures (referring to intrauterine devices, oral contraceptives and obstruction measures); 2. Patients with severe heart disease, such as: decompensated heart failure (NYHA stage III and IV); unstable angina pectoris; history of myocardial infarction within the past 12 months, etc.; 3. Patients with secondary hyperuricemia caused by blood disease, kidney disease or tumor radiotherapy and chemotherapy; 4. Brain disease, abnormal judgment ability; mental illness unable to cooperate; 5. Alcohol or drug addicts; 6. Those who have participated in other clinical trials within three months before the screening of this trial; 7. Malignant tumor, active tuberculosis; 8. Complicated with other diseases, and the researchers believe that it affects the evaluation of efficacy or poor compliance; 9. Those taking glucocorticoid drugs; 10. White blood cell count < 3.0x10^9/L, or platelets < 100x10^9/L, or hemoglobin < 90g/L; 11. For any other reason, the investigator considers it inappropriate to participate in the trial; 12. Those who are allergic to all the drugs in this test or their ingredients, or have existing allergies, or have hypersensitivity constitution.

Design outcomes

Primary

MeasureTime frame
Fasting blood routine;Coagulation;Blood sugar;Islet autoantibodies (GAD, IAA, ICA) titers;

Countries

China

Contacts

Public ContactHou Xu

Shandong Provincial Hospital

15153285655@163.com+86 15153285655

Outcome results

None listed

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