FindTrial
Sign In

Preoperative quantitative sensory testing in remote pain-free areas for predicting axial pain after posterior cervical spinal surgeries

Preoperative quantitative sensory testing in remote pain-free areas for predicting axial pain after posterior cervical spinal surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200056260
Enrollment
Unknown
Registered
2022-02-03
Start date
2017-01-01
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Postoperative axial pain

Interventions

PAP group:none

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. A confirmed diagnosis of multilevel cervical pathologies including CSM or OPLL; 2. A surgical history of posterior cervical decompression.

Exclusion criteria

Exclusion criteria: 1. Previous spinal surgery, cervical structural pathologies (e.g., trauma, infections and tumor); 2. Coexisting conditions that could increase procedural risk or worsen/change the pain (e.g., severe hypertension or cardiac disease, peripheral vascular disease, shoulder impairment, and neurological disease).

Design outcomes

Primary

MeasureTime frame
Quantitative sensory testing;—

Countries

China

Contacts

Public ContactZheng Chaojun

Huashan Hospital, Fudan University

countd2388@163.com+86 13564635319

Outcome results

None listed

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