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NCT07556497Recruiting

Role of Endothelial Progenitor Cells Dysregulation and Inflammation in the Pathophysiology of Cardiovascular Complications of Type 2 Diabetes

Source: ClinicalTrials.gov · Last updated 29 Apr 2026

Brief summary (registry, in English)

This study aims to isolate endothelial progenitor cells (EPCs) from participants with type 2 diabetes (T2D) and cardiovascular complications and to comprehensively characterize EPC dysfunction. Specifically, the study will evaluate maladaptive angiocrine signaling, calcium signaling pathways, and the role of inflammation in EPC function and the progression of atherosclerosis during T2D development. A sub-study will assess EPC functionality by examining endothelial nitric oxide synthase (eNOS) expression and activity, as well as the effectiveness of in vitro eNOS gene enhancement.

Status (registry)
Recruiting
Study type
Observational
Enrollment
90 (estimated)
First submitted
13 Apr 2026
Start date
17 Nov 2020
Primary completion date
31 Dec 2026
Lead sponsor
Weill Cornell Medical College in Qatar
NCT number
NCT07556497

What you commit to

  • Study type: Observational
  • Planned participants: 90
  • From 17 Nov 2020 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Type I diabetes, MODY diabetes or other form of diabetes
  • Active infection, inflammation, cancer or acute illness of any kind (other than a cardiovascular complication of diabetes if applicable in the group they are assigned to).
  • Chronic inflammation (eg. auto-immune diseases) or infections (eg. HIV, chronic hepatitis).
  • Evidence of malignancy within the past 5 years

Other

  • Unable to meet the inclusion criteria

Who the study is looking for

  • T2D
  • Males and females
  • Older than 18 years of age
  • Willingness to participate in the study and provide written consent form
  • Consent to having peripheral blood withdrawals and urine collection for the study requirement.

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hamad Medical Corporation
Coordinator of this site? Confirm its status
DohaQatarRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.