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CompletedNo phase

Ultra-low Dose Contrast for Endovascular Procedures

Key facts

Who runs it
Attikon Hospital
Where
Greece1 site in 1 countryChoose a country to see its sites
Trial code
Status
Completed
People taking part
18 people enrolled
Started
1 Sept 2024
Ended
23 Jan 2026
Type of study
Observational
Treatments tested
  • Infrainguinal peripheral endovascular revascularization
Record updated
10 March 2026

Who can take part

Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 9 criteriaShow less

Who can take part

  • CLTI
  • Prescheduled infrainguinal revascularization procedure
  • Renal disease stage 2-4 (eGFR <60ml/minute/1.73m2)
  • Adequate pre- and post-procedural hydration protocol

Who cannot take part

  • End-stage renal disease/ dialysis
  • Endovascular treatment of Iliac artery steno-oclussive disease
  • Allergy to contrast media
  • eGFR >60ml/minute/1.73m2)
  • Inadequate pre- and post-procedural hydration protocol

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

The purpose of this protocol is to study the safety and feasibility of using ultra-low dose iodinated contrast agent for infrainguinal endovascular revascularization procedures in patients with chronic limb-threatening lower limb ischemia (CLTI) and impaired renal function, in the new angiography suite of our department.

The group in the trial

  • Study cohort

    Patients with renal disease stages 2-4, scheduled to undergo infrainguinal endovascular procedures due to CLTI, using ultra-low dose of iodine contrast media.

    Treatment: Infrainguinal peripheral endovascular revascularization

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Feasibility Study of the Use of Ultra-low Dose Iodinated Contrast Agent for Endovascular Procedures in Patients With Chronic Limb-threatening Ischemia and Renal Impairment
Record updated
10 March 2026