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Status unknownNCT02385409Updated Mar 11, 2015

Incidence and Reasons for Preoperative Anemia in Elective Lower Joint Arthroplasty

An observational study in Anemia, Arthroplasty, Replacement, Hip and Arthroplasty, Replacement, Knee, sponsored by Oeivind Jans. Status unknown at 1 site in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-03-11.

Sponsored by Oeivind Jans · Observational

The sponsor has not verified this record recently (last verified Mar 2015), so the status shown — last known as Active, not recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
900
Ages
18 Years and older
Sex
All
01

Study summary

Preoperative anemia is an independent risk factor for the need for allogeneic transfusion during surgery and increased postoperative morbidity.

Treatment of preoperative anemia is recommended. However the type of preoperative anemias in elective hip- and knee surgery has only been sparsely studied.

This observational study aims to investigate the incidence and type of anemias prior to elective hip- and knee arthroplasty.

Read the detailed description

Preoperative anemia is an independent risk factor for the need for allogeneic transfusion during surgery and increased postoperative morbidity.

In elective orthopedic surgery, international guidelines recommends treatment of preoperative anemia including the use of Iron supplements for anemias associated with iron deficiency. In addition, low iron stores in both anemic and non-anemic patients may delay postoperative hemoglobin recovery.

However, the reasons for preoperative anemia and the prevalence of patients with low iron stores have only been sparsely studied in elective hip- and knee arthroplasty.

This observational study aims to investigate the incidence and type of anemias prior to elective hip- and knee arthroplasty.

02

Conditions studied

  • Anemia
  • Arthroplasty, Replacement, Hip
  • Arthroplasty, Replacement, Knee

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Keywords

  • Patient Blood Management
  • Preoperative anemia
  • Hip replacement
  • Knee replacement
03

In context

Anemia

1,733 studies on the registry are indexed under Anemia; 246 are open to participants now.

This study's planned enrollment of 900 is above the median of 200 across 326 observational studies indexed under Anemia.

Browse Anemia studies →

Lead sponsor

This is the only study on the registry with Oeivind Jans as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All patients scheduled for elective primary hip- and knee replacement during a 1 year sampling period at the department of orthopedic surgery, Hvidovre Hospital, Denmark

Inclusion criteria

  • Age > 18 years
  • Scheduled for elective primary hip- or knee replacement.

Exclusion criteria

Exclusion Criteria:

  • Not possible to obtain preoperative blood sample.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
900 participants (estimated)
Patient registry
No

Groups and cohorts

  • Elective Total Hip- or Knee arthroplasty patients

    Patients scheduled for elective Hip- or knee replacement at Hvidovre Hospital, Denmark.

06

What researchers measure

Primary outcomes

  1. Anemia Classification - Biochemical classification from preoperative venous blood samples

    Biochemical classification from preoperative venous blood samples

    Time frame: Date of preoperative blood sampling

Secondary outcomes

  1. Prevalence of Anemia according to WHO definitions

    According to WHO definitions

    Time frame: Date of preoperative blood sampling

  2. Proportions of non-anemic patients with low irons stores

    Low Ferritin or Transferin saturation (TSAT)

    Time frame: Date of preoperative blood sampling

07

Study locations

1 site
  • Hvidovre Hospital, Department of orthopaedic surgery
    Hvidovre, 2650, Denmark
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 11, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02385409
Lead sponsor
Oeivind Jans
Collaborators
Hvidovre University Hospital
Responsible party
Oeivind Jans (M.D., Ph.D., Rigshospitalet, Denmark) — Sponsor-investigator
First posted
Mar 11, 2015
Start date
May 2013
Primary completion
May 2014
Completion
May 2015 (estimated)
Last update
Mar 11, 2015

Study contacts

Øivind Jans, M.D., Ph.D.
study director · Rigshospitalet, Denmark

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2015. You cannot join it, but the record below documents what was studied.

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