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临床试验/NL-OMON24365
NL-OMON24365招募中不适用

Cross-Education After ACL Reconstruction

niversity Medical Center Groningen0 个研究点目标入组 50 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Patients awaiting an ACL reconstruction surgery will be included: male, female, age 20 to 60, any race, BMI < 30 kg/m2, time between injury and surgery < 1 year, ACL tear to the dominant or non-dominant leg with or without meniscal excision, hamstring autograft, allograft of any source, signed informed consent, and follow study protocol.

排除标准

  • If they are pregnant (surgeon will look in the medical record of the patient), have an injury to the other leg, a meniscal tear requiring repair, additional interventions that interfere with standard rehab (e.g., cartilage lesion treatment), multiple serious injuries to target leg (ACL tear+meniscus tear, ACL+plus collateral ligament tear, prior
  • major surgery to legs, pelvis), revision ACL reconstruction on the same knee, degenerative arthritis on radiographs or articular cartilage fissures extending to subchondral bone, or exposed bone as seen in arthroscopy (grade IV), current or prior neurological conditions (Parkinson’s disease, stroke, dementia).

研究者

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