Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 10:58 AM
Ignite Modification Date:
2025-12-26 @ 10:58 AM
NCT ID:
NCT06984406
Eligibility Criteria:
Inclusion Criteria:
* Age ≥18 years.
* Planned PCI.
* High risk of CIN with:
1. eGFR according to the CKD-EPI formula \<60 ml/min/1.73 m2 or
2. At least two of the following criteria: liver damage (cirrhosis), diabetes mellitus, age \>70 years, administration of contrast in the last 7 days, CHF (LVEF \>40%), intake of drugs affecting renal function (ACE inhibitors, ARBs, NSAIDs, aminoglycosides, diuretics).
* Signing informed consent.
Exclusion Criteria:
* Allergy to nitrates.
* Acute coronary syndrome.
* Acute condition accompanied by systolic blood pressure \<90 mmHg for more th an 30 minutes or requiring the use of drugs with a positive inotropic effect.
* Life-threatening conditions requiring emergency medical care.
* Participation in other clinical trials.
* Pregnancy, lactation.
* Use of nitrates in the last 30 days.
* Abuse of alcohol, illegal drugs, mnestic-intellectual decline, as well as other reasons and circumstances indicating expected low adherence to treatment.
* Refusal to follow the plan of visits and examinations provided for by the protocol of this clinical trial.
* Refusal to sign informed consent.
* Infectious diseases.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06984406
Study Brief:
Protocol Section:
NCT06984406