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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05364398
Other study ID # MD-09-2017
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2017
Est. completion date September 1, 2020

Study information

Verified date May 2022
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To assess the clinical outcome in patients who had ACL reconstruction with preservation of the remnant and compare it with patients in whom the stump was resected


Description:

100 patients are subjected to ACL reconstruction. Half of them had ACL reconstruction with Stump preservation and the other half had ACL reconstruction with stump resection. The clinical outcome in both groups is assessed and compared


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date September 1, 2020
Est. primary completion date April 30, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - patients with torn ACL within 6 months Exclusion Criteria: - Old ACL injury Multi-ligamentous knee injuries Mal-alignments

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ACL reconstruction
Use of hamstring tendons graft to replace the torn ACL and being passed and fixed through the femoral and tibial sides

Locations

Country Name City State
Egypt Kasr Alainy, Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Knee stability KT-1000 Arthrometer after 2 years
Primary Knee proprioception Passive angle reproduction test after 2 years
Primary Lysholm score After 2 years
Primary Tegner activity score after 2 years
Primary IKDC score after 2 years
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