Status:
RECRUITING
"Erectile Function After PCI in MI and Non-MI Patients"
Lead Sponsor:
Kırıkkale University
Conditions:
Erectile Disfunction
Coronary Artery Disease (CAD)
Eligibility:
MALE
30-75 years
Brief Summary
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)...
Detailed Description
In Thıs study, we aım to evaluate the erectile status of male patients undergoing percutaneous coronary intervention after both heart attack ( group 1) and stable angina ( Group 2). The primary aim i...
Eligibility Criteria
Inclusion Criteria
-
Male patients aged 30-75 years
-
Undergoing successful percutaneous coronary intervention (PCI) for one of the following:
- Acute myocardial infarction (Group 1)
- Stable angina (Group 2)
-
Hemodynamically stable after the PCI procedure
-
Survival of the index hospitalization
-
Ability to provide written informed consent
-
Sexually active within the 3 months prior to enrollment
-
Willingness and ability to complete follow-up visits and questionnaires at:
- Baseline (post-PCI recovery)
- 3 months
- 6 months Exclusion Criteria
-
Known malignancy (active or recently treated)
-
Neurological disorders affecting erectile function, including:
- Spinal cord injury
- Multiple sclerosis
- Parkinson's disease
-
Uncontrolled diabetes mellitus (HbA1c > 9%)
-
Presence of more than two chronic systemic diseases, such as:
- Severe renal disease
- Severe hepatic disease
- Severe pulmonary disease
-
Polypharmacy, defined as chronic use of more than three daily medications
-
Absence of sexual activity or lack of a sexual partner
-
Refusal or inability to provide informed consent or complete study questionnaires
-
Severe psychiatric illness interfering with study participation
-
Endocrine disorders, including:
- Untreated hypogonadism
- Thyroid disease
-
Major post-PCI complications preventing participation, including:
- Reinfarction
- Stroke
- Heart failure
Key Trial Info
Start Date :
January 15 2026
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
November 1 2026
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT07444697
Start Date
January 15 2026
End Date
November 1 2026
Last Update
March 3 2026
Active Locations (1)
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1
The Hospital of Kirikkale Univerity Faculty of Medicine
Kirikkale, Turkey (Türkiye), 71450