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临床试验/CTRI/2026/04/108476
CTRI/2026/04/108476尚未招募不适用

App to Preoperatively Measure Hamstring Tendon Length and Thickness in Patients Planned for Arthroscopic ACL Repair

DR TALAL HASAN JUMIRUL HUSSAIN1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2026年4月24日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
100
试验地点
1

研究概览

简要总结

Anterior cruciate ligament (ACL) reconstruction using hamstring tendon autograft requires adequate graft length and diameter for optimal surgical outcomes. Intraoperative measurement of graft size may lead to uncertainty and need for alternative graft options. This study aims to develop and validate a mobile application that predicts hamstring tendon length and diameter preoperatively using MRI-based and/or anthropometric parameters. Patients undergoing primary arthroscopic ACL reconstruction will be prospectively enrolled. Preoperative graft size predicted by the mobile application will be compared with actual intraoperative graft measurements. The study intends to evaluate the accuracy, correlation, and clinical utility of the application in predicting graft adequacy, thereby improving preoperative planning and reducing intraoperative uncertainty.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients diagnosed with anterior cruciate ligament (ACL) tear planned for primary arthroscopic ACL reconstruction using hamstring tendon autograft.
  • Patients with preoperative MRI of the affected knee available for measurement of hamstring tendon parameters.
  • Patients willing to provide written informed consent for participation in the study.
  • Patients with intact hamstring tendons and no prior ligament reconstruction in the affected knee.

排除标准

  • Patients undergoing revision ACL reconstruction or with history of previous ACL surgery.
  • Patients with multiligament knee injury or associated major knee pathology.
  • Patients with congenital or acquired musculoskeletal deformity affecting lower limb.
  • Patients with inadequate / poor-quality MRI or MRI not available.
  • Patients with contraindication to MRI.
  • Patients unwilling to provide informed consent.

研究者

发起方
DR TALAL HASAN JUMIRUL HUSSAIN
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

DR TALAL HASAN JUMIRUL HUSSAIN

Saveetha Medical College And Hospital

研究点 (1)

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