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observation of prevention of tibia tunneling

Evaluation of the effectiveness of placing the proximal 1/3 anterior cruciate ligament stump in individuals with complete anterior cruciate ligament rupture in preventing an increase in tibial tunnel diameter: a randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200802048270N1
Enrollment
30
Registered
2021-11-12
Start date
2021-11-22
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

disruption of anterior cruciate ligament of knee. Other spontaneous disruption of anterior cruciate ligament of knee

Interventions

Intervention 1: Patients who during surgery, 1/3 of the proximal remnants of the anterior cruciate ligament (ACL) stump remain in the tibial canal. Intervention 2: Control group: Patients without prox

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 18 to 40 years old complete anterior cruciate ligament Consent to participate in the study

Exclusion criteria

Exclusion criteria: history of previous surgery due to anterior cruciate ligament injury History of surgery on other lower limbs

Design outcomes

Primary

MeasureTime frame
Tibial canal diameter change 1. Timepoint: The diameter of the tibial tunnel is measured during the operation and 12 months after the operation. Method of measurement: The diameter of the tibial tunnel is measured during surgery and 12 months after surgery using a CT scan by an orthopedic surgeon.

Secondary

MeasureTime frame
Frequency of anterior sliding test negative. Timepoint: 12 months after surgery. Method of measurement: Clinical examinations.;Frequency of negative pivot-shift test. Timepoint: 12 months after surgery. Method of measurement: Clinical examinations.;Lysholm scale score. Timepoint: 12 months after surgery. Method of measurement: Lysholm scale questionnaire.;Ikdc scale score. Timepoint: 12 months after surgery. Method of measurement: Ikdc scale questionnaire.;Frequency of Lachman test negative. Timepoint: 12 months after surgery. Method of measurement: Clinical examinations.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAhmad Azizi

Iran University of Medical Sciences

azizi3981@gmail.com+98 21 8214 1000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026