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

The feasibility of home monitoring for patients undergoing outpatient surgery for elective hip or knee replacement - HORATIO: Home monitoring after outpatient primary hip or knee Prosthesis

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON51009

Enrollment

Registered

2021-12-21

Start date

2022-04-18

Completion date

Unknown

Last updated

2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

joint degeneration Osteoartritis

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Primary unilateral THA, TKA or UKA Preoperative body mass index (BMI)

Exclusion criteria

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

Design outcomes

Primary

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

Secondary

Measure	Time frame
Secondary Objective: Patient satisfaction measured with a patient satisfaction survey (5- point Likert scale) Tertiary Objective: Cost effectiveness. A cost analysis will be conducted by the Diakonessenhuis Finance Department.	—

Countries

Netherlands

Outcome results