Measurement of Nardilysin concentration in synovial fluid

Measurement of Nardilysin concentration in synovial fluid - Measurement of Nardilysin concentration in synovial fluid

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000051872

Enrollment

Registered

2023-08-09

Start date

2023-07-14

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Rheumatoid arthritis, knee osteoarthritis, meniscus injury, ligament injury

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients undergoing total knee replacement surgery or knee arthroscopic surgery at Shiga University of Medical Science Hospital Orthopedic Surgery during the study period, or patients requiring outpatient knee joint puncture 2. Gender does not matter 3. Age of 18 years old or older at the time of obtaining consent 4. Consent to participate in research can be obtained from the person in writing

Exclusion criteria

Exclusion criteria: 1. Those who cannot consent to participate in this study 2. Subjects with severe anemia (hemoglobin 8g/dL or less) 3. Patients who are judged by the principal investigator or co-investigators to be inappropriate as subjects of this study

Design outcomes

Primary

Measure	Time frame
Between-group comparison of Nardilysin levels in synovial fluid and serum	—

Countries

Japan

Contacts

Public ContactYasutaka Amano

Shiga University of Medical Science Department of Orthopaedic Surgery

amano021@belle.shiga-med.ac.jp077-548-2562

Outcome results