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临床试验/NCT03289104
NCT03289104撤回不适用

Improving Sternal Healing After Cardiac Surgery: Sternal Wire vs ZIPFIX

Ottawa Heart Institute Research Corporation2 个研究点 分布在 1 个国家开始时间: 2018年9月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
2
主要终点
Sternal bone healing

研究概览

简要总结

The objective of this study is to determine whether sternal reconstruction using the ZIPFIX system compared to standard wire cerclage could improve bone healing, patient function, and decreased postoperative pain.

详细描述

Despite a longer time for bone healing and functional recovery, median sternotomy is still the most common approach in cardiac surgery. Sternal closure has traditionally been wire cerclage using stainless steel wires, however, new sternal fixation devices have been developed to improve sternal union. Rigid sternal fixation, although very costly, has demonstrated to be superior to standard wire cerclage both in clinical and biomechanical studies. Although improved sternal healing was observed with rigid plate fixation in a randomized controlled trial in high risk patients, the wound complication rate with plate fixation was almost double that of wire cerclage albeit not statistically significant.

A novel sternal closure system denoted the sternal ZIPFIX system (DePuySynthes, Companies of Johnson and Johnson, West Over, PA, US) is biocompatible Poly-Ether-Ether-Ketone implant that was developed for fast and reliable sternal fixation following median sternotomy. First published case series utilized the sternal ZIPFIX System demonstrating effective sternal stability at 30 days. Another study has demonstrated no significant difference in the incidence of sternal wound infection following the ZIPFIX system compared to standard wire cerclage while Stelly et al., 2015 demonstrated reduced risk of deep sternal wound infection for patients using ZIPFIX. The ZIPFIX system demonstrates a higher resistance of fatigue failure and has a larger implant-to-bone contact area compared to stainless steel wires thereby reducing the risk of bone cut through. Placement of the cable ties are done similar to wire cerclage thereby not affecting time for sternal closure and training.

The objective of this study is to determine whether sternal reconstruction using the ZIPFIX system compared to standard wire cerclage would improve bone healing, patient function, and decrease postoperative pain.

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
Single (Participant)

入排标准

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

入选标准

  • Patient age ≥ 18 years
  • Scheduled cardiac surgery including coronary artery bypass grafting, aortic valve replacement, mitral valve replacement/repair, or ascending aorta replacement.
  • Patient undergoing elective or urgent surgery
  • Ability to understand study procedures and to comply with them for the entire length of the study.

排除标准

  • Patients undergoing emergent cardiac surgery
  • Severe congestive heart failure (NYHA class III or IV) at enrollment
  • Prior cardiac surgery
  • Patients undergoing ventricular assist device insertion or heart transplantation
  • Patients with a known metal allergy or allergy to ZIPFIX implant
  • Patients who refuses consent
  • Patients who are unable to follow post-operative instructions
  • Prior history of significant bleeding that might be expected to recur with cardiac surgery
  • Dementia with a mini mental status examination (MMSE) score of < 20
  • Extra cardiac illness that is expected to limit survival to less than 5 years
  • Suspected pregnancy. A pregnancy test (urine or serum) will be administered to all women not clearly menopausal
  • Concurrent enrollment in another clinical trial
  • Geographic inaccessibility for follow-up visits required by the protocol
  • Prisoners or institutionalized individuals

研究组 & 干预措施

Steel Wires

Active Comparator

In this arm, patients will have their sternum closed with steel wires.

干预措施: Steel Wires (Device)

ZipFix Sternal Closure System (Plastic Cables)

Experimental

In this arm, patients will have their sternum closed with the ZipFix system.

干预措施: ZipFix Sternal Closure System (Device)

结局指标

主要结局

Sternal bone healing

时间窗: 3 months after surgery

Assessment of how the sternum is healing, assessed via a CT scan and classified using a 6-point scale.

次要结局

  • Post-operative pain(Within 1 week of surgery)
  • Use of narcotics(In the first 6 months after surgery)
  • Cost(In the first 6 months after surgery.)
  • Sternal wound infection(In the first 6 months after surgery)
  • Sternal instability(In the first 6 months after surgery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Marc Ruel MD MPH FRCSC

Chief Cardiac Surgeon

Ottawa Heart Institute Research Corporation

研究点 (2)

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