Actively Recruiting
"Erectile Function After PCI in MI and Non-MI Patients"
Led by Kırıkkale University · Updated on 2026-03-03
100
Participants Needed
1
Research Sites
41 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this observational study is to assess changes in patients' erectile function after percutaneous coronary intervention (PCI) using a standard IIEF (International Index of Erectile Function) questionnaire at 1, 3, and 6 months post-PCI. By doing this, we try to compare patients' responses to PCI after having a heart attack and stable angina to see the real effect of myocardial infarction on erectile function status in the long term by comparing it with a very similar group.
CONDITIONS
Official Title
"Erectile Function After PCI in MI and Non-MI Patients"
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male patients aged 30-75 years
- Undergoing successful percutaneous coronary intervention (PCI) for acute myocardial infarction or stable angina
- Hemodynamically stable after PCI procedure
- Survived the initial hospitalization
- Able to provide written informed consent
- Sexually active within the 3 months before enrollment
- Willing and able to complete follow-up visits and questionnaires at baseline, 3 months, and 6 months
You will not qualify if you...
- Known active or recently treated malignancy
- Neurological disorders affecting erectile function such as spinal cord injury, multiple sclerosis, or Parkinson's disease
- Uncontrolled diabetes mellitus with HbA1c greater than 9%
- More than two chronic systemic diseases including severe renal, hepatic, or pulmonary disease
- Chronic use of more than three daily medications (polypharmacy)
- No sexual activity or lack of a sexual partner
- Refusal or inability to provide informed consent or complete study questionnaires
- Severe psychiatric illness interfering with participation
- Endocrine disorders including untreated hypogonadism or thyroid disease
- Major post-PCI complications such as reinfarction, stroke, or heart failure
AI-Screening
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Trial Site Locations
Total: 1 location
1
The Hospital of Kirikkale Univerity Faculty of Medicine
Kirikkale, Turkey (Türkiye), 71450
Actively Recruiting
Research Team
T
Timucin Sipal, MD, PhD
CONTACT
C
Caglar Alp, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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