Clinical Trials Directory

Trials / Unknown

UnknownNCT06030791

BTB Graft Harvest and Donor Site Morbidity After ACL Reconstruction

The Impact of Bone-tendon-bone Graft Harvest and Biological Regeneration of Bone-tendon Defects on the Development of Donor Site Morbidity After Anterior Cruciate Ligament Reconstruction

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Clinical Center of Vojvodina · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers

Summary

The aim of this observational study is to examine the connection between bone-tendinous defects after BTB graft harvest and the development of anterior knee pain.

Detailed description

The purpose of this study is to investigate the impact of bone-tendinous defects after ACL reconstruction on the development of anterior knee pain. We will assess the presence and extent of bone-tendinous defects using MRI scans, which will be conducted at two time points: 4 weeks and 1 year after ACL reconstruction surgery. Furthermore, we will compare the healing progress of the bone-tendinous defects observed on the MRI scans. In addition, we will evaluate the correlation between the residual bone-tendinous defect and knee functionality by comparing the results with knee functional test (IKDC form, Lysholm score, Donor site morbidity score). All individuals participating in the study have provided their informed consent by signing the necessary documents prior to their inclusion in the research.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTMRIMRI of operated knee

Timeline

Start date
2022-10-31
Primary completion
2024-10-31
Completion
2024-10-31
First posted
2023-09-11
Last updated
2023-09-11

Locations

1 site across 1 country: Serbia

Source: ClinicalTrials.gov record NCT06030791. Inclusion in this directory is not an endorsement.