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Peri-articular injection for Pain Relief After Anterior Cruciate Ligament Reconstructio

Not Applicable
Recruiting
Conditions
Diseases of the musculo-skeletal system and connective tissue
Registration Number
KCT0003572
Lead Sponsor
Chung-Ang University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
34
Inclusion Criteria

Patients from 19 to 60 years of age who underwent primary anterior cruciate ligament reconstruction at Chung-Ang University Hospital and can cooperate in collecting data

Exclusion Criteria

Patients with an American Society of Anesthesiologist grade 3 or higher
A previous history of previous knee surgery or reconstruction of other ligaments
Patients who underwent autogenous reconstruction of the anterior cruciate ligament, re-reconstruction of anterior cruciate ligament, or concomitant high tibial osteotomy
Patients who have allergies or contraindications of medication used in this study for pain control and those who do not consent to use
Patients who are constantly using analgesics regardless of the study
Patients who have serious cardiovascular, kidney disease, hematologic abnormalities, obesity (BMI> 35)

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual analog scale
Secondary Outcome Measures
NameTimeMethod
pain VAS score (Visual analog scale);use of rescue medication,;side effects;patient satisfaction with pain control
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