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Postoperative Anemia and Functional Outcomes After Fast-track Primary Hip Arthroplasty

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Rigshospitalet

Status

Completed

Conditions

Anemia
Arthroplasty, Hip Replacement

Study type

Observational

Funder types

Other

Identifiers

NCT01514006
H-4-2011-117

Details and patient eligibility

About

The purpose of this study is to evaluate the possible association between postoperative anaemia and functional outcomes the first 2 weeks after primary hip arthroplasty.

The investigators hypothesise that patients with a higher degree of postoperative anaemia have impaired postoperative rehabilitation as measured by standardized functional outcome tests.

Full description

Postoperative anemia may impair postoperative rehabilitation due to anemia related symptoms such as fatigue or dizziness. Although, the impact of postoperative anemia on postoperative rehabilitation and function has previously been examined the results are conflicting.

Patients undergoing fast-track hip arthroplasty (THA) are mobilized early and participate in physiotherapy during the admission but are discharged early (2-3) days postoperative. However, the ability to rehabilitate early after discharge has not been evaluated in relation to postoperative anemia.

The purpose of this observational study is to evaluate the possible association between postoperative anaemia and functional outcomes the first 2 weeks after primary hip arthroplasty.

The investigators hypothesise that patients with a higher degree of postoperative anaemia have impaired postoperative rehabilitation as measured by standardized functional outcome tests. Hb concentrations and functional outcome measurements will be performed preoperatively, at the day of hospital discharge and during a postoperative visit 12-16 days after surgery.

Enrollment

125 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing primary unilateral THA
  • Age 65 or older

Exclusion criteria

  • Not able to give consent
  • Not able to walk prior to surgery
  • Chronic need for RBC transfusion

Trial design

125 participants in 1 patient group

Study Cohort
Description:
Patients, aged 65 or above, undergoing elective primary unilateral hip arthroplasty in a fast-track setting.

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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