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临床试验/NCT02964754
NCT02964754已完成不适用

Digital Three-dimensional Imaging Models for Repair of Complex Long Bone Fractures: a Randomized Controlled Trial With 6-month Follow-up

Qinghai University0 个研究点目标入组 63 人开始时间: 2014年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
63
主要终点
X-ray examination

研究概览

简要总结

To verify whether digital three-dimensional model-assisted internal fixation can obtain better effects in the repair of complex long bone fractures compared with conventional internal fixation.

详细描述

History and current related studies The internal fixator is difficult to completely fit the bone surface at the site of complex long bone fracture, which reduces the firmness of fixation. From a safety point of view, the establishment of a digital three-dimensional measurement model is undoubtedly a very reliable and intuitive way. Digital three-dimensional models are established after CT scan, and these models can greatly reflect the site and degree of fractures, and reduce anatomical parameters, with high degree of simulation and feasibility.

Adverse events

  1. The investigators will record adverse events, including screw loosening and falling off, steel plate fracture and bending, joint stiffness, delayed healing or non-healing, peripheral nerve injury and infection.
  2. If severe adverse events occur, investigators will report details, including the date of occurrence and measures taken to treat the adverse events, to the principle investigator and the institutional review board within 24 hours.

Data collection, management, analysis and open-access

  1. Data collection: Case report forms with demographic data, disease diagnosis, accompanying diseases, drug allergy history, and adverse events will be collected, processed using Epidata software (Epidata Association, Odense, Denmark), collated, and then recorded electronically by data managers using a double-data entry strategy.
  2. Data management: The locked electronic database will be accessible and locked only by the project manager, and will not be altered. All data regarding this trial will be preserved by the Affiliated Hospital of Qinghai University, China.
  3. Data analysis: The electronic database will be statistically analyzed by a professional statistician who will create an outcome analysis report that will be submitted to the lead researchers. An independent data monitoring committee will supervise and manage the trial data, ensuring a scientific and stringent trial to yield accurate and complete data.
  4. Data open access: Anonymized trial data will be published at www.figshare.com.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Long bone fractures in the four limbs, such as middle segment of humerus, femur, ulna, radius, tibia and fibula; fractures are not related to the articular surface
  • Diagnosed with complex long bone fractures via X-ray
  • Admission within 6 hours after injury

排除标准

  • Pathological fractures with vascular and nerve injuries
  • Split fractures of the humeral head
  • Neer IV fractures
  • Humeral head compression area greater than 40%
  • Glenohumeral dislocation
  • Conscious disturbance, cerebral infarction, tumor, serious medical complications, such as heart, lung, kidney failure, severe hypertension, diabetes and blood diseases
  • History of elbow joint dysfunction or shoulder joint disease
  • Unwilling to sign the informed consent

研究组 & 干预措施

the observation group

Experimental

32 patients with complex long bone fractures will be randomized to undergo digital three-dimensional models will be established by CT scan for internal fixation in the observation group.

干预措施: CT scan for internal fixation (Device)

the control group

Experimental

31 patients will be randomized to undergo conventional internal fixation in the control group.

干预措施: conventional internal fixation (Procedure)

结局指标

主要结局

X-ray examination

时间窗: postoperative 6 months

To evaluate total efficacy at postoperative 6 months

次要结局

  • Harris scores(preoperatively and 6 months postoperatively)
  • Visual Analogue Scale(preoperatively and 6 months postoperatively)

研究者

发起方
Qinghai University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zichun Zhao

Associate Chief Physician

Qinghai University

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