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临床试验/DRKS00010246
DRKS00010246尚未招募未知

Anterior cruciate ligament reconstruction with autologous semitendinosus- or quadriceps tendon graft: Are there differences in objective and subjective patients' outcome? A randomized controlled trial. - QuadSemiT

niversitätsklinikum Münster0 个研究点目标入组 60 人开始时间: 2016年4月11日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Open (masking not used)

入排标准

年龄范围
16 Years 至 60 Years(—)
性别
All

入选标准

  • Primary rupture of anterior cruciate ligament (for randomization)
  • - for the accessory controll group (study arm No 3, ACL Revision with Quadriceps tendon graft) a rerupture after primary ACL reconstruction/suture is inclusion criterion
  • - Age 16-60 years
  • - Signed informed consent, study and privacy agreements
  • - Succesfully completed all standard preoperative procedures especially from anaesthesological und surgical point of view
  • - Willing to participate on follow-up examinations.
  • - Minor concomitant injuries such as small meniscus lesions (<1/3 partial meniscectomy or minor sutures), I-II° MCL instability, bone bruise without relevant chondral lesions or hemarthros are acceptable for inclusion.

排除标准

  • - No compliance
  • - Denial of participating in rehabilitation program
  • - Severe traumatic or degenerative chondral or meniscal injuries
  • - Multiligamental injuries/instability of higher grades (LCL, PCL or III° MCL)
  • - Prior donation/extraction of tendon grafts at the same leg (except for the study arm No 3 / ACL Revision group if quadriceps tendon is still available)
  • - Relevant co-medication or co-morbidities
  • - Pregnancy

研究者

发起方
niversitätsklinikum Münster

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