Clinical trial

Pain Management of Anterior Cruciate Ligament Reconstruction: Evaluation of Adductor Canal Block Versus Oral Pain Regimen

Name
1115203
Description
This study will compare the outcome of pain interventions that are considered standard of care during the surgical treatment of ACL injuries. The comparison will be looking at pain control during and after ACL surgery as well as functional outcomes in patients that had a nerve block versus those who did not. The investigators hypothesize that pain control will be equal between both groups.
Trial arms
Trial start
2017-10-09
Estimated PCD
2024-07-01
Trial end
2024-07-01
Treatment
Adductor Canal Nerve Block
An adductor canal nerve block with 15 mL of 0.5% ropivacaine will be performed pre-operatively by Anesthesiology.
Arms:
Adductor Canal Nerve Block
Ropivacaine injection
15 mL of 0.5% ropivacaine will be administered for the adductor canal block
Arms:
Adductor Canal Nerve Block
Size
60
Primary endpoint
Immediate Post-op Pain Score
15 min post-op
Opioid Use
6 weeks post-op
Eligibility criteria
Inclusion Criteria: * Between the ages of 18 and 45 years old. * Clinical and/or advanced imaging confirmation of ACL tear of which reconstructive surgery is recommended and accepted. Exclusion Criteria: * No prior surgery of the affected and contralateral knee * Adults unable to consent * Children (age \< 18 years old) * Prisoners * Pregnant women * Inflammatory arthritis * Non-English-speaking patients
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'DOUBLE', 'maskingDescription': 'Operating surgeon and outcome assessor will be blind to whether patient had nerve block prior to OR.', 'whoMasked': ['INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 60, 'type': 'ESTIMATED'}}
Updated at
2024-05-17

1 organization

1 product

1 indication