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Mechanism of cartilage degeneration induced by circPVT1/miR-125b/Cbfß on the pathogenesis of osteoarthrsis

Mechanism of cartilage degeneration induced by circPVT1/miR-125b/Cbfß on the pathogenesis of osteoarthrsis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300075101
Enrollment
Unknown
Registered
2023-08-25
Start date
2023-08-25
Completion date
Unknown
Last updated
2023-08-28

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

Conditions

Osteoarthritis

Interventions

Control group:None

Sponsors

The Affiliated Hospital of Guizhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: Experimental group (pathological cartilage): All sexes, age >60 years, severe knee osteoarthritis with total knee replacement surgery, study diagnosis and surgical treatment criteria refer to: Chinese Medical Association Orthopaedic Branch "Guidelines for the diagnosis and treatment of osteoarthritis" (2018 edition), AAOS "Evidence-based medical guidelines for osteoarthritis of the knee (2013 second edition) Control group (normal cartilage): gender and age are not limited

Exclusion criteria

Exclusion criteria: 1. Chronic consumptive diseases such as tumors and tuberculosis; 2. Other types of bone and joint diseases such as gout and rheumatoid arthritis; 3. Congenital deformity and dysfunction of knee joint caused by congenital factors; 4. People with mental illness can't cooperate with researchers; 5. Menstrual and pregnancy women; 6. With a history of knee joint infection and surgical trauma; 7. With a history of articular cavity puncture and injection therapy; 8. With a history of drugs such as hormone free and immunosuppressive drugs; 9. With serious systemic diseases and no obvious abnormalities in liver, renal function and electrolytes. Control group (normal cartilage): Patients with previous diagnosis of osteoarthritis, severely injured amputees with normal articular cartilage, severely injured first-stage joint replacement patients, and deceased donor patients.

Design outcomes

Primary

MeasureTime frame
circPVT1;miR-125b;Cbfß;Interleukin;TNF-a;MMPs;COMP;

Secondary

MeasureTime frame
YKL-40;CTX-?;ACAN;hsa_circ_0023404;HIF-1a;VEGF;Bcl-2;collagen II;aggrecan;ADAMTS-4;ADAMTS-5;PCNA;CD14;ACTG1;HLA-DRA;COL6A3;Col6a1;Col1a1;

Countries

China

Contacts

Public ContactLi Guangdi

The Affiliated Hospital of Guizhou Medical University

leegd@foxmail.com+86 136 1858 5566

Outcome results

None listed

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