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Application of cytokine antibody array technology in screening serum markers of postoperative discitis

Application of cytokine antibody array technology in screening serum markers of postoperative discitis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-RPC-17012892
Enrollment
Unknown
Registered
2017-10-06
Start date
2017-11-01
Completion date
Unknown
Last updated
2017-10-09

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

Conditions

postoperative discitis

Interventions

experimental group:Non intervention study
Disease control group:Non intervention study
Negative control group:Non intervention study

Sponsors

Quanzhou Orthopedic-traumatological Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. A definite history of lumbar surgery; 2. Diagnosis as lumbar intervertebral disc infection after lumbar surgery combining with the medical history, symptoms, signs and the related examination, MRI for example.

Exclusion criteria

Exclusion criteria: 1. Pregnant women. 2. Complicated with severe cardiovascular, liver, kidney, hematopoietic system diseases, autoimmune diseases, or poor nutritional status. 3. patients with failed lumbar surgery syndrome.

Design outcomes

Primary

MeasureTime frame
cytokine antibody array technology;—

Countries

China

Contacts

Public ContactYANG Shengping

Quanzhou Orthopedic-traumatological Hospital

yang_shengping@hotmail.com+86 15159590965

Outcome results

None listed

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