Status:

UNKNOWN

Intravenous Iron Supplement to Prevent Postoperative Delirium After Hip Fracture Surgery

Lead Sponsor:

Seoul National University Bundang Hospital

Collaborating Sponsors:

JW Pharmaceutical

Conditions:

Hip Fractures

Eligibility:

All Genders

65+ years

Phase:

PHASE4

Brief Summary

This is a clinical trial to evaluate the effect of intravenous iron supplement with Ferinject (Ferric Carboxymaltose) in preventing postoperative delirium after hip fracture surgery.

Detailed Description

We hypothesized that IV iron supplement will (1) decrease postoperative delirium in hip fracture patients and (2) decrease the amount of transfusion and transfusion-related complications.

Eligibility Criteria

Inclusion

  • femur neck fracture, intertrochanteric fractures
  • Iron deficiency anemia (Hb\<12 in women, Hb\<13 in men)
  • Iron deficiency (Serum ferritin \<100ug/L or transferrin saturation\<20%)
  • Who understands this clinical trial and volunteers and agrees to this trial

Exclusion

  • Patient under the age of 65 years
  • Hb\<7 or someone who has acute symptom of anemia(tachycardia, dyspnea, or dizziness)
  • High energy trauma
  • Preoperative delirium
  • MMSE\<10
  • Underlying disease which involves cognitive dysfunction (e.g. neurovascular diseases, acute myocardial infarction, pulmonary embolism)
  • Those who are inappropriate to participate in the clinical trial assessed by the investigators

Key Trial Info

Start Date :

July 30 2020

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 31 2024

Estimated Enrollment :

264 Patients enrolled

Trial Details

Trial ID

NCT05429749

Start Date

July 30 2020

End Date

December 31 2024

Last Update

June 23 2022

Active Locations (1)

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1

Seoul National University Bundang Hospital

Seongnam, South Korea, 13620