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Comparison Study of Outpatient and Routine Hip and Knee Arthroplasty and Patient Recovery Trajectory: A Randomized Crossover Study Protocol

Comparison Study of Outpatient and Routine Hip and Knee Arthroplasty and Patient Recovery Trajectory: A Randomized Crossover Study Protocol

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116809
Enrollment
Unknown
Registered
2026-01-15
Start date
2026-01-18
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Hip and Knee Joint Diseases

Interventions

outpatient group:Choose outpatient mode for joint replacement

Sponsors

Xi'an Honghui Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1: Patients planned to undergo bilateral hip or knee replacement surgery, with an interval of no more than 36 months between the two surgeries 2: Age 18-75 years old, gender unrestricted 3: American Society of Anesthesiologists (ASA) classification grade I-III, no severe systemic disease or systemic disease controlled and stable 4: Meets the criteria for day surgery admission, including: a robust family support system (with at least one caregiver available to provide continuous assistance for 3 days post-discharge) and convenient emergency return access to the hospital. 5: Normal cognitive function, with good communication skills, able to understand the research content and complete the questionnaire evaluation 6: voluntarily participate in this study and sign the informed consent form

Exclusion criteria

Exclusion criteria: 1: Accompanied by neuromuscular system diseases (such as severe myasthenia gravis, sequelae of poliomyelitis, Parkinson's disease, etc.) affecting joint function evaluation 2: patients with inflammatory joint diseases such as rheumatoid arthritis and ankylosing spondylitis 3: Merged cognitive impairment or mental illness unable to cooperate in completing questionnaire evaluation 4: Use of glucocorticoids or immunosuppressants within one month before surgery 5: Known or suspected allergy to prosthesis materials (polyethylene, titanium, cobalt, chromium, molybdenum, etc.) 6: Body Mass Index (BMI) > 40 kg/m^² 7: accompanied by local or systemic active infectious foci

Design outcomes

Primary

MeasureTime frame
PROs;Joint Function Score;

Secondary

MeasureTime frame
30s-CST;Visual analogue scale, VAS;Physical Activity Level;

Countries

China

Contacts

Public ContactLi Zheng

Xi'an Honghui Hospital

leezheng08@163.com+86 130 9696 6117

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026