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临床试验/NCT02989363
NCT02989363Unknown不适用

Evaluation of the Use of Resources and Costs With O-arm in Brain Stimulation Deep Surgeries and Complex Back Surgeries

Instituto de Investigacion Sanitaria La Fe1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2011年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
80
试验地点
1
主要终点
Costs of health resources (stays, visits, diagnostic and therapeutic tests, personnel, consumables and implants) with DBS (O-Arm and without O-Arm groups)

研究概览

简要总结

Evaluation of the use of resources and costs with O-arm in deep brain stimulation (DBS) surgeries and complex back surgeries

详细描述

To measure the use of health resources in application A (with DBS) and in application B (vertebral fusions), in patients in the intervention group with O-arm and in the control group (usual care without O-arm) with the cost in each phase (pre-surgical, surgical, post-surgical and follow-up at 6 months (RAQUIS) and at 12 months (DBS))

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

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

入选标准

  • •Patients aged ≥18 years.
  • •Signed informed consent.
  • •Patients with indication for DBS surgery for movement disorders, epilepsy and obsessive-compulsive disorder, or for cervical, dorsal or lumbar fusion surgery levels 1,2 and 3 in a degenerative disease

排除标准

  • •Patients who have had pediatric instrumented surgery.
  • •Patients in which the pedicle screws are inserted for neoplasia or other disease.

研究组 & 干预措施

O-Arm in deep brain stimulation surgeries (DBS)

Experimental

Use of image surgery with technology O-Arm in deep brain stimulation surgeries (DBS)

干预措施: Device O-Arm in DBS (Procedure)

Control group Not O-Arm in deep brain stimulation surgeries

Experimental

Not use of image surgery with technology O-Arm in deep brain stimulation surgeries (DBS)

干预措施: Not device O-Arm in DBS (Procedure)

O-Arm in complex back surgeries (RAQUIS)

Experimental

Use of image surgery with technology O-Arm in complex back surgeries (RAQUIS)

干预措施: Device O-Arm in RAQUIS (Procedure)

Control group Not O-Arm in complex back surgeries (RAQUIS)

Experimental

Not use of image surgery with technology O-Arm in complex back surgeries (RAQUIS)

干预措施: Not device O-Arm in RAQUIS (Procedure)

结局指标

主要结局

Costs of health resources (stays, visits, diagnostic and therapeutic tests, personnel, consumables and implants) with DBS (O-Arm and without O-Arm groups)

时间窗: 12 months

Costs of health resources (stays, visits, diagnostic and therapeutic tests, personnel, consumables and implants) with vertebral fusions (O-Arm and without O-Arm groups)

时间窗: 6 months

次要结局

  • Safety of surgeries in the intervention groups (DBS) measured like rate of surgical re-intervention(12 months)
  • Safety of surgeries in the control group (RAQUIS) measured like rate of complications associated with surgery(6 months)
  • Safety of surgeries in the intervention groups (DBS) measured like rate of complications associated with surgery(12 months)
  • Quality of life related to health in the intervention group (DBS) measured with the EQ-5D questionary(12 months)
  • Accuracy of surgeries in the control group (RAQUIS) measured with the rate of electrode or thyroid replacement during surgery(6 months)
  • Accuracy of surgeries in the intervention group (DBS) measured with the rate of electrode or thyroid replacement during surgery(12 months)
  • Safety of surgeries in the control group (RAQUIS) measured like rate rate of surgical re-intervention(6 months)

研究者

发起方
Instituto de Investigacion Sanitaria La Fe
申办方类型
Other
责任方
Sponsor

研究点 (1)

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