Trials / Recruiting
RecruitingNCT07055152
Retinal OCTA for Microvascular Dysfunction Evaluation and Outcome Prediction in MINOCA Patients
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 90 (estimated)
- Sponsor
- University of Pisa · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Accepted
Summary
The aim of this study is to evaluate microvascular dysfunction through OCTA in MINOCA patients. In order to better understand the condition, OCTA will also be performed in two matched patient groups: healthy controls and ACS patients. The study will compare the retinal microvascular parameters across these groups to determine differences in microvascular function in MINOCA patients. Additionally, in the MINOCA subgroup, the study will further evaluate the differences in microvascular dysfunction within specific subsets of patients (e.g., Takotsubo, vasospastic angina, microvascular angina, patients with evidence of plaque erosion) to understand the variability and potential mechanisms underlying each subgroup of MINOCA.
Conditions
Timeline
- Start date
- 2025-01-01
- Primary completion
- 2026-01-01
- Completion
- 2027-01-01
- First posted
- 2025-07-08
- Last updated
- 2025-07-08
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT07055152. Inclusion in this directory is not an endorsement.