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Clinical Trials/NCT05369325
NCT05369325
Completed
N/A

Accuracy of Non-invasive Hemoglobin Monitoring in Patients Undergoing Outpatient Total Joint Arthroplasty

Mayo Clinic1 site in 1 country200 target enrollmentJune 15, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Total Joint Arthroplasty
Sponsor
Mayo Clinic
Enrollment
200
Locations
1
Primary Endpoint
Concordance between non-invasive Hgb and serum Hgb
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

This research is being done to better understand the accuracy of noninvasive hemoglobin tests on patients that recently underwent total joint arthroplasty.

Registry
clinicaltrials.gov
Start Date
June 15, 2022
End Date
July 1, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Matthew P. Abdel, M.D.

Principal Investigator

Mayo Clinic

Eligibility Criteria

Inclusion Criteria

  • Adult patients age ≥
  • Undergoing either primary total knee or total hip arthroplasty for a primary underlying diagnosis of osteoarthritis.

Exclusion Criteria

  • Individuals \< 18 years of age.

Outcomes

Primary Outcomes

Concordance between non-invasive Hgb and serum Hgb

Time Frame: 1 hour

How closely the non-invasive and serum Hgbs correlate with one another statistically

Patient satisfaction with non-invasive Hgb

Time Frame: 1 day

Patients will get a survey to fill out following the Hgb measurements that assesses their satisfaction with the non-invasive method

Nurse satisfaction with non-invasive Hgb

Time Frame: 1 day

Nurses will get a survey to fill out following the Hgb measurements that assesses their satisfaction with the non-invasive method

Cost comparison between non-invasive and serum Hgb

Time Frame: 1 year

We will analyze cost differences between the non-invasive Hgb devices and the serum lab tests

Study Sites (1)

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