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Combination of decompression with instrumentation and chemotherapy for eosinophilic granuloma of the pediatric spine:a prospective study

Combination of decompression with instrumentation and chemotherapy for eosinophilic granuloma of the pediatric spine:a prospective study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-POC-17012420
Enrollment
Unknown
Registered
2017-08-19
Start date
2010-01-01
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

eosinophilic granuloma

Interventions

Surgical group:Surgical treatment of decompression with instrumentation, chemotherapy and adjuvant therapy.
Control group:chemotherapy and adjuvant therapy

Sponsors

Shanghai Changzheng Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 15 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria include the pediatric patients younger than 15 years old with pathological diagnosis of spinal eosinophilic granuloma, and had primary treatment in our institution. Their epiphyseal plate should be premature and the structure of vertebral body are destroyed by the imaging examinations (including magnetic resonance imaging (MRI) and computed tomography (CT)).

Exclusion criteria

Exclusion criteria: Exclusion criteria include the patients with non-spine lesions or systematic Langerhans cell histiocytosis (LCH), without pathological diagnosis of eosinophilic granuloma, older than 15 years old or with epiphyseal plate closure under imaging examinations. Patients with serious spinal cord compression or spinal instability, who cannot have conservative treatment, or with the contraindications of surgical treatment are not included in our study. The patients who have poor compliance with incomplete chemotherapy, have primary treatment elsewhere, are participating other randomized controlled trials (RCT), or loss to follow-up are also excluded from our study.

Design outcomes

Primary

MeasureTime frame
central height of vertebral body;length of vertebral pedicle;sagittal diameter of spinal canal;transverse diameter of spinal canal;Cobb's angle;VAS scale;Oucher scale;Frankel scale;

Secondary

MeasureTime frame
height;bone maturity;use of analgesics;duration of immobilization. ;

Countries

China

Contacts

Public ContactJianru Xiao

Shanghai Changzheng Hospital

jianruxiao83@163.com+86 13701785283

Outcome results

None listed

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