The feasibility of home monitoring for patients undergoing outpatient surgery for elective hip or knee replacement

Completed

• Conditions: joint degeneration; Osteoartritis; 10023213

• Registration Number: NL-OMON51009
• Lead Sponsor: Diakonessenhuis Utrecht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

Primary unilateral THA, TKA or UKA
Preoperative body mass index (BMI)<40 kg/m2
Age 18-75 years at the time of surgery

Exclusion Criteria

ASA score IV
Revised cardiac risk score > 2
Predictive Postoperative Nausea and Vomiting (Apfel) score > 2
Cognitive impairment (e.g. Dementia)
Use of psychopharmaceutical medicine
Chronic obstructive pulmonary disease with FEV1 <= 1
Obstructive sleep apnoea

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Primary Objective:<br /><br>The primary outcome is the mean percentage of successful wireless transmissions<br /><br>from home of blood pressure (BP) levels, heart rate (HR), respiratory rate<br /><br>(RR), oxygen saturation (SpO2) levels, temperature and pain score up to and<br /><br>including postoperative day 4 with a feasibility target of >=90%.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary Objective:<br /><br>Patient satisfaction measured with a patient satisfaction survey (5- point<br /><br>Likert scale)<br /><br><br /><br><br /><br>Tertiary Objective:<br /><br>Cost effectiveness. A cost analysis will be conducted by the Diakonessenhuis<br /><br>Finance Department.</p><br>