Assessment for efficacy of anterior cruciate ligament reconstruction using oval dilator system
Not Applicable
- Conditions
- Injury, poisoning and certain other consequences of external causes
- Registration Number
- KCT0007139
- Lead Sponsor
- Chung-Ang Univerisity Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 112
Inclusion Criteria
patients who underwent ACL reconstruction at our hospital, those aged 19 to 60 who can cooperate with data collection
Exclusion Criteria
Patients with grade 3 or higher of the American Society of Anesthesiologists
Patients with fractures requiring open reduction and internal fixation.
Patient with a history of previous knee surgery.
Patient with multiple ligament injuries.
Patient who have performed other procedures, such as high tibial osteotomy.
A person undergoing reconstruction of the anterior cruciate ligament.
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Radiological -Knee anterior drawer pull view (Telos stress device) ;physical exam - Knee range of mortion/Pain (VAS)/Anterior drawer test/ posterior drawer test/pivot-shift test/ Lachman test
- Secondary Outcome Measures
Name Time Method Questionnaire - IKDC objective/subjective score, Lysholm score, Tegner score