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Study of Single And Double Bundle Anterior Cruciate Ligament (ACL) Graft Cross-sectional Dimensions

Study of Single And Double Bundle ACL Graft Cross-sectional Dimensions Compared With Native ACL

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02834962
Enrollment
100
Registered
2016-07-15
Start date
2016-07-31
Completion date
2017-08-31
Last updated
2016-07-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rupture of Anterior Cruciate Ligament

Keywords

Anterior Cruciate Ligament Reconstruction

Brief summary

To study the difference between single and double bundle ACL graft cross-sectional dimensions compared with native ACL using postoperative 3-D MRI.

Detailed description

The investigators divide 100 patients with ACL rupture into 2 groups. Group A undergo single bundle anterior cruciate ligament reconstruction (ACLR). Group B undergo double bundle ACL reconstruction. At 3-6 weeks post operation, all the patients undergo 3-D MRI examination of both knees. The investigators reconstruct 3-D models of reconstructed ACL and native ACL, and compare the difference between single and double bundle graft.

Interventions

anterior cruciate ligament reconstruction using single bundle technique

anterior cruciate ligament reconstruction using double bundle technique

Sponsors

Peking University Third Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
10 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* ACL rupture patients aged between 10 to 50 years

Exclusion criteria

* combined severe injuries to the operated knee (additional ligament rupture, major meniscus loss, patella instability, cartilage damage \>2°, pathologic leg axis deviation) * any injury or surgery to the contralateral knee * any inflammatory or systemic disease, neuromuscular disease in the lower limbs,any recent knee infection

Design outcomes

Primary

MeasureTime frame
long to short axis ratio of the cross-sectional area of the reconstructed ACL3-6 weeks
long axis of the cross-sectional area of the reconstructed ACL3-6 weeks
short axis of the cross-sectional area of the reconstructed ACL3-6 weeks
cross-sectional area of the reconstructed ACL3-6 weeks

Contacts

Primary ContactYu Jia-Kuo, MD
yujiakuo@126.com86-10-82267392
Backup ContactLiu Yang, MD
surgeonliuyang@sina.com86-10-82267019

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026