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:
2025-12-24 @ 10:08 PM
Ignite Modification Date:
2025-12-24 @ 10:08 PM
NCT ID:
NCT01947335
Eligibility Criteria:
Inclusion Criteria:
* Written informed consent
* Age \>=18 years
* Coronary artery disease scheduled for percutaneous intervention
* Technical feasibility for intravascular ultrasound to guide coronary angioplasty
* Increased risk for contrast-induced acute renal failure (e.g. age \> 80 years, female gender, diabetes, urgent or emergent procedure priority, diabetes, congestive heart failure, increased baseline serum creatinine, decreased calculated or measured creatinine clearance, intra-aortic balloon pumping, previous renal transplantation or single kidney)
Exclusion Criteria:
* Anticipated technical impossibility for intravascular ultrasound
* Unknown baseline renal function
* Baseline end-stage renal failure needing dialysis
* Acute renal failure with dynamic change in renal function at the time of index procedure
* Iodine contrast administration \<= 72 prior to index procedure
* Known allergy to iodine contrast
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01947335
Study Brief:
Protocol Section:
NCT01947335