NCT04114708

MRI Review of ACLR With and Without Lateral Extra-articular Tenodesis

• Status: Withdrawn
• Phase: N/A
• Study type: Interventional
• Enrollment: 0 (actual)
• Sponsor: NYU Langone Health · Academic / Other
• Sex: All
• Age: 13 Years – 25 Years
• Healthy volunteers: Not accepted

Summary

The purpose of the proposed study is to evaluate the effect of lateral extra-articular tenodesis (LET) on anterior cruciate ligament reconstruction through evaluation of postoperative magnetic resonance imaging (MRI). This will be a single-center non-randomized controlled study. The study is comparing postoperative graft MRI findings in two cohorts: patients undergoing isolated ACLR and patients undergoing ACLR with lateral extra-articular tenodesis (LET). Postoperative MRIs will be obtained at 6, 9 and 12 months postoperatively.

Conditions

• Ruptured Achilles Tendon

Interventions

Type	Name	Description
DIAGNOSTIC_TEST	Anterior cruciate ligament Reconstruction (ACLR)	All patients will undergo an anatomic ACLR via a standardized fashion using BTB autograft.
DIAGNOSTIC_TEST	ACLR with lateral extra-articular tenodesis (LET)	All LETs will be performed in a standardized fashion using the modified Lameire technique. All patients will undergo an anatomic ACLR via a standardized fashion using BTB autogaft graft.

Timeline

• Start date: 2022-01-01
• Primary completion: 2022-10-01
• Completion: 2022-10-01
• First posted: 2019-10-03
• Last updated: 2022-07-08

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study