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Vildagliptin recruits regulatory T cells in patients undergoing primary percutaneous coronary intervention

Vildagliptin recruits regulatory T cells in patients undergoing primary percutaneous coronary intervention - vildagliptin and regulatory T cells

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00014045
Enrollment
60
Registered
2018-02-15
Start date
2017-10-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

MedDRA - Myocardial infarction MedDRA - Diabetes

Interventions

Group 1: Control group (diabetic patients with STEMI n = 30 ) was given the standard medical treatment (Aspirin 300 mg once daily , low molecular weight heparin 0.5 mg/kg/day IV , and clopidogrel 600

Sponsors

Faculty of medicine - Tanta university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 59 Years

Inclusion criteria

Inclusion criteria: diabetic patients with STE MI

Exclusion criteria

Exclusion criteria: Patients were excluded from the study if they had any one of the following criteria: previous myocardial infarction, previous PCI or coronary artery bypass intervention, were currently on DPP- 4 inhibitors, steroidal and non- steroidal anti-inflammatory drugs, has long term immunosuppressive therapy, cancer and infectious diseases.

Design outcomes

Primary

MeasureTime frame
What? the addition of vild to standard medical treatment of MIRI (myocardial ischaemia-reperfusion injury) could increase the effectiveness of it through recruitment of CD4+CD25+ Treg cells. How? Through the assessment of percentage of changes in nitric oxide, ischemia modified albumin, highly sensitive C reactive protein and interferon gamma levels, myeloperoxidase activity, CD4 +CD25+ Treg cells count and Transforming growth factor-beta1 level in the studied groups. When? It is measured twice for each patient; reading 1 is baseline reading at time of admission before starting the treatment and reading 2 measured 72 hours after starting the medical treatment.

Countries

Egypt

Contacts

Public ContactFatma H Rizk

Faculty of medicine - tanta university

Fatma.rezk@med.tanta.edu.eg+2- 01064122556,

Outcome results

None listed

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