跳至主要内容
临床试验/NCT00931333
NCT00931333终止2 期

Non Comparative, Monocentric, Prospective, Phase II, Study of Calcium Phosphate Cement MCPC Efficacy and Safety for Bone Filling in Vertebral Site

University Hospital, Bordeaux2 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2009年7月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
终止
发起方
入组人数
4
试验地点
2
主要终点
The efficiency of non-percutaneous vertebroplasty using MCPC, in 18 to 65 years old patients, after a huge trauma, will be evaluated based on evaluation of the vertebra height by measuring local traumatic angle.

研究概览

简要总结

The macroporous calcium phosphate cement, MCPC, which composition is close to bone, is malleable and biocompatible, and has intrinsic radio opacity and good ability to undergo mechanical constraints. After the filling of the bone cavity, the cement hardens. Interestingly, this calcium phosphate cement has no exothermic hardening (on the contrary, the ordinary cements used nowadays cause necrotic lesions in tissues around during this phase) and favours vascularisation, cellular colonisation and bone healing. Thanks to its resorbability, the MCPC cement is replaced little by little by a physiologic bone. This last property is very important for young people needing a vertebroplasty after a traumatism.

Thus, it will be tested in a low-invasive surgery, a non-percutaneous vertebroplasty, consisting in filling with the MCPC the body of the broken vertebra, after its stabilization thanks to 4 interpedicular screws. This protocol will be proposed to patients 1 to 3 weeks after the trauma having caused the fracture.

The follow up will last 12 months with 5 visits (2 days, and 3, 4, 6 and 12 months after vertebroplasty), 2 CT scanners before inclusion and at 12 months, 2 EOS (ultra low dose imager replacing classical radiography) at 5 and 12 months, questionnaires (visual analogic scale for pain, and quality of life with OSWESTRY and SF36 scales) before inclusion and at 2 days, and 3, 4, 6 and 12 months, and biological exams (CRP/VS, for inflammation) at each visit except 2 days after surgery. An osteodensitometry will be performed at 3 months.

详细描述

The macroporous calcium phosphate cement, MCPC, which composition is closer to bone than acrylic cement, is malleable and biocompatible, and has intrinsic radio opacity and good biomechanical properties (12 +/- 3 Mpa in 24 hours). After the filling of the bone cavity, the cement hardens in situ thanks to hydrolysis and apatite precipitation. Interestingly, this calcium phosphate cement has no exothermic hardening (on the contrary, the PMMA causes necrotic lesions in tissues around during this phase). During the dissolution, a macroporosity takes form between biphasic calcium phosphate granules. That permits vascularisation, cellular colonisation and bone healing. Thanks to its resorbability, the MCPC cement is replaced by a physiologic tissue. This last property is very important for young people needing a vertebroplasty after a traumatism.

The issue is to validate this biomaterial with appropriate mechanical, biocompatibility properties and intrinsic radio opacity, and that can favour bone regeneration, with a lower frequency of leak and risk enhancement of other vertebra fracture. The MCPC will thus be tested on few patients to assess its efficacy and security for bone filling in vertebra site.

Thus, it will be used in a low-invasive surgery, a non-percutaneous vertebroplasty, consisting in filling with the MCPC the body of the broken vertebra, after its stabilization thanks to 4 interpedicular screws. This protocol will be proposed to 21 patients 1 to 3 weeks after the trauma having caused the fracture. The follow up will last 12 months with 5 visits.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged between 18 and 65 years old, BMI < 30
  • Stable and important fracture of the vertebral body between T9 and L5
  • Diagnostic maximum 3 weeks after the trauma causing the fracture
  • Type A1 to A3 (MAGERL scale) assessed by CT scan
  • Lumbar local traumatic angle > 10°, and thoracic > 15°
  • Given informed consent
  • Patient with French health system

排除标准

  • For women: no efficient contraception (intra uterine device, or contraceptive pill)
  • Pregnant or feeding women
  • Fractures due to metastasis or multiple myeloma
  • Symptomatic compression of the spinal cord
  • Multi site vertebroplasty
  • Scoliosis with a Cobb angle > 20°
  • Surgery zone local infection
  • All surgical contraindications
  • Immune system abnormalities, immune deficiency or suppression, HIV or BHV or CHV (positive serology)
  • Severe hyperparathyroidism: calcium > 2,45 mmol/l and [PTH] ≥ 50pg / ml
  • Uncontrolled diabetes (untreated or non stabilized by treatment)
  • Long corticoid treatment (more than 6 months and stopped since less than 3 months)
  • Chemotherapy
  • All contra indication to MCPC: osteomyelitis, bone degenerative disease or necrosis of surgery site.
  • Known allergy to indigotine

研究组 & 干预措施

1

Experimental

干预措施: non percutaneous vertebroplasty (Procedure)

结局指标

主要结局

The efficiency of non-percutaneous vertebroplasty using MCPC, in 18 to 65 years old patients, after a huge trauma, will be evaluated based on evaluation of the vertebra height by measuring local traumatic angle.

时间窗: At the 4th month after the surgical procedure

次要结局

  • The proportion of Severe Adverse Events frequency (cement leak, new fractures, late huge loss of vertebra height) and inflammatory response(before inclusion and at 3 months, 4 months, 5 months, 12 months)
  • Pain intensity: difference between before inclusion and during follow up. Evaluation with Visual Analogic Scale.(before inclusion and at 2 days, and 3, 4, 6 and 12 months)
  • Quality of life: difference between before inclusion and during follow up. Evaluation with OSWESTRY and SF 36 scales.(before inclusion and at 2 days, and 3, 4, 6 and 12 months.)
  • The evolution of bone formation and MCPC resorption: quantification of bone reconstruction.(CT scan at 6 and 12 months after surgery, and with osteodensitometry at 3 months after surgery)

研究者

发起方
University Hospital, Bordeaux
申办方类型
Other
责任方
Sponsor

研究点 (2)

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