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Epidemiological investigation and clinical intervention evaluation of central sensitization in knee arthroplasty candidates

Epidemiological investigation and clinical intervention evaluation of central sensitization in knee arthroplasty candidates

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031674
Enrollment
Unknown
Registered
2020-04-06
Start date
2020-04-04
Completion date
Unknown
Last updated
2020-04-13

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

Conditions

knee arthroplasty,central sensitization

Interventions

A:Central sensitization patients(Medicine for central sensitization)
B:Central sensitization patients(placebo)
C:Normal patients (No-treatment Control)

Sponsors

Department of Joint Surgery, Ningbo Sixth Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with severe knee osteoarthritis waiting for replacement surgery,; 2. Aged 50 years or older; 3. Objects of culture above primary school; 4. Participants who voluntarily participate in the study and can provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. People with mental disorder, personality disorder and substance abuse / dependence; 2. Subjects who refused to participate in the study due to stress events in the past week; 3. Subjects who did not have knee replacement surgery, patients who use non surface replacement joint prosthesis.

Design outcomes

Primary

MeasureTime frame
Knee Osteoarthritis Outcome Score, KOOS;Visual Analogue Scale/Score, VAS;Central Sensitization Inventory, CSI;

Secondary

MeasureTime frame
knee function (HHS, ROM, WOMAC);complication;

Countries

China

Contacts

Public ContactLing Jing

Ningbo Sixth Hospital

lingjing07@163.com+86 18906628636

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 23, 2026