NCT05489952

Brief Summary

Geriatric hip fracture is an important disease that affects the health life of the elderly in China. Geriatric hip fracture is often complicated by a variety of comorbidities due to advanced age. And anemia is a common comorbidity. At present perioperative management of geriatric hip fracture, transfusion is only indicated for moderate and severe anemia, while no special medical intervention for mild anemia in China. More and more studies have found that iron can not only correct anemia, but also improve cardiac function, patients' quality of life and function. This study investigated the effect of perioperative iron supplementation on activity tolerance in elderly patients with hip fracture complicated with iron deficiency anemia. The study was a randomized, parallel controlled clinical study. Due to the requirements of the ethics committee, the unblinded setting was cancelled due to ethical considerations. Research will be grouped according to whether to accept iron supplementation treatment, are divided into 2 groups, respectively, iron treatment group and the traditional method. The method of randomization was stratified block randomization. The experimental group added to the intravenous iron sucrose during perioperative period according to the degree of iron deficiency. If there is still a iron deficiency or anemia at discharge, oral ferrous lactate is added after discharge. The outcomes include 6-minute walk distance, Harris score, EQ-5D score six months after surgery, perioperative blood transfusion rate, and so on in the two groups.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
444

participants targeted

Target at P75+ for phase_4

Timeline
Completed

Started Sep 2022

Typical duration for phase_4

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 31, 2022

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 5, 2022

Completed
1 month until next milestone

Study Start

First participant enrolled

September 15, 2022

Completed
2.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 15, 2025

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 15, 2025

Completed
Last Updated

September 22, 2022

Status Verified

September 1, 2022

Enrollment Period

2.4 years

First QC Date

July 31, 2022

Last Update Submit

September 21, 2022

Conditions

Outcome Measures

Primary Outcomes (1)

  • 6-minute walk distance

    The 6-minute walk distance (6 MWD) provides a measure for integrated global response of multiple cardiopulmonary and musculoskeletal systems involved in exercise. The 6 MWT provides information regarding functional capacity, response to therapy and prognosis across a broad range of chronic cardiopulmonary conditions.

    6 months

Secondary Outcomes (2)

  • Harris hip score

    6 months

  • perioperative blood transfusion rate

    1 week

Study Arms (2)

iron supplement group

EXPERIMENTAL
Drug: iron sucrose and ferrous lactate

control group

NO INTERVENTION

Interventions

The experimental group added to the intravenous iron sucrose during perioperative period according to the degree of iron deficiency. If there is still a iron deficiency or anemia at discharge, oral ferrous lactate is added after discharge.

Also known as: iron supplementation
iron supplement group

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

You may qualify if:

  • \>65 years old patients with hip fracture
  • Patients with iron deficiency or anemia,
  • preoperative hemoglobin \<13g/ dL in males and \<12g/ dL in females, and \>9g/ dL,
  • serum ferritin \< 100 ng/ mL or serum ferritin 100-299 ng/ mL or transferrin saturation (TSAT) \<20%

You may not qualify if:

  • Coronary artery bypass grafting, percutaneous transluminal coronary angioplasty, and cardiac device implantation (including cardiac resynchronization) within preoperative 30 days
  • Acute coronary syndrome, transient ischemic attack or stroke occurred within 30 days before surgery;
  • Refused to sign the consent form to be included in the clinical trial group;
  • Can't walk before injury;
  • Use erythropoietic preparation within 3 months before surgery and oral iron preparation within 4 weeks 30 days before surgery(\> 100 mg/ day)
  • Patients with liver and kidney dysfunction

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shenzhen Second People's Hospita

Shenzhen, Guangdong, 518035, China

RECRUITING

MeSH Terms

Conditions

Hip FracturesOsteoporotic Fractures

Interventions

Ferric Oxide, Saccharatedferrous lactate

Condition Hierarchy (Ancestors)

Femoral FracturesFractures, BoneWounds and InjuriesHip InjuriesLeg Injuries

Intervention Hierarchy (Ancestors)

Ferric CompoundsIron CompoundsInorganic ChemicalsGlucaric AcidSugar AcidsAcids, AcyclicCarboxylic AcidsOrganic ChemicalsHydroxy AcidsCarbohydrates

Study Design

Study Type
interventional
Phase
phase 4
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

July 31, 2022

First Posted

August 5, 2022

Study Start

September 15, 2022

Primary Completion

February 15, 2025

Study Completion

August 15, 2025

Last Updated

September 22, 2022

Record last verified: 2022-09

Locations