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IMPACT OF INTRAVENOUS IRON TREATMENT OF PREOPERATIVE ANEMIA IN PATIENTS WITH LOWER EXTREMITY PERIPHERAL ARTERY DISEASE (IRONPAD)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-514593-50-00
Acronym
IRONPAD
Enrollment
240
Registered
2024-05-22
Start date
2019-06-06
Completion date
Unknown
Last updated
2024-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anemia in patients with chronic ischemia of the lower limb ischemia

Brief summary

Reduce the incidence of transfusion from randomization up to 30 days after the main surgery in patients with anemia who undergo revascularization surgery with chronic lower limb ischemia

Detailed description

- Establish the optimal preoperative time of highest yield of iv iron to increase HB. - Changes and evolution of hemoglobin during admission; difference in Hb between inclusion, intervention and discharge. Hb 30 days after discharge. - Impact of anemia and its treatment on length of hospital stay, morbimortality and quality of life during admission and first 30 postoperative days

Interventions

Sponsors

Asociacion Instituto De Investigacion Sanitaria Biobizkaia
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Reduce the incidence of transfusion from randomization up to 30 days after the main surgery in patients with anemia who undergo revascularization surgery with chronic lower limb ischemia

Secondary

MeasureTime frame
- Establish the optimal preoperative time of highest yield of iv iron to increase HB. - Changes and evolution of hemoglobin during admission; difference in Hb between inclusion, intervention and discharge. Hb 30 days after discharge. - Impact of anemia and its treatment on length of hospital stay, morbimortality and quality of life during admission and first 30 postoperative days

Countries

Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026