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Impact of postoperative early time-dependent back-lumbalis muscle exercise on central sensitization in patients with failed back surgery syndrome

Impact of postoperative early time-dependent back-lumbalis muscle exercise on central sensitization in patients with failed back surgery syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055961
Enrollment
Unknown
Registered
2022-01-29
Start date
2018-02-01
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

failed back surgery syndrome

Interventions

FBSS group:None
Non-FBSS group:None
normal group:none

Sponsors

Huashan Hospital Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 95 Years

Inclusion criteria

Inclusion criteria: FBSS patient group: 1. A clear history of anatomically and technically successful lumbosacral spinal surgery; 2. Increased/persistent pain in the lumbosacral area with or without radiation to the leg for at least 6 months after the operation; 3. LBP intensity at rest and/or with movement greater than or equal to 3 on the 0 to 10 numeric rating pain scale (NRS; 0 = no pain, 10 = maximum tolerable pain). Patient-control group: Not exhibit chronic LBP after lumbosacral spinal surgery. Normal-control group: Matched for demographic data in relation to the patient group, and these healthy subjects must not have presented episodes of LBP for more than 7 days in the last 12 months.

Exclusion criteria

Exclusion criteria: 1. Lumbar structural pathologies (e.g., traumatic spinal injuries, infections, tumor, and ankylosing spondylitis); 2. Coexisting conditions that could increase procedural risk or worsen/change the pain (e.g., severe hypertension or cardiac disease, peripheral vascular disease, diabetes mellitus, sepsis, coagulopathy, coexisting chronic pain, peripheral or central neurological disease, and drug or alcohol abuse); 3. Psychiatric or other conditions that would disturb the subject's cooperation; 4. Incomplete medical records; 5. Patients who were lost to follow-up.

Design outcomes

Primary

MeasureTime frame
Quantitative Sensory Testing, QST;Pain-related scales;psychosocial questionnaires;

Countries

China

Contacts

Public ContactZheng Chaojun

Huashan Hospital Fudan University

countd2388@163.com+86 21 52887136

Outcome results

None listed

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