FNB in ACL Recon Under SA

ConditionsAnterior Cruciate Ligament Rupture Femoral Nerve Block

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age19-60

SponsorChuncheon Sacred Heart Hospital

About this trial

The investigators will compare the results of sono-guided femoral nerve block in arthroscopic surgery for anterior cruciate ligament reconstruction under spinal anesthesia.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

individuals who are scheduled to undergo arthroscopic anterior cruciate ligament reconstruction surgery and must be received sufficient explanation about the research prior to surgery and have provided their informed consent to participate.

Disqualifiers

who require simultaneous surgery for concomitant cartilage injury, medial meniscus tear, and lateral collateral ligament tear.

who have previously undergone surgical treatment within the knee joint.

who have declined to participate in the research.

where medical, surgical, or anesthetic complications occurred during surgery.

Trial design

Design model

Parallel

Treatments tested in this trial

Sono-guided injection
Procedure/Surgery
After spinal anesthesia, patients will be injected around femoral nerve using ultrasonography.
Ropivacaine injection
Drug
After spinal anesthesia, patients will be injected 20ml ropivacaine around femoral nerve.
Saline injection
Drug
After spinal anesthesia, patients will be injected 20ml 0.9% saline around femoral nerve.

Treatment groups

100 Participants

are divided into 2 treatment groups

Group A: FNBExperimental treatment 2 interventions

Group B: no FNBPlacebo comparator 2 interventions

Trial outcomes

Primary outcomes

postoperative pain after 24hours

VAS (Visual analog scale) measured 24 hours after operation * the unabbreviated scale title: The visual analog scale * the minimum and maximum values: 0, 10 * higher scores mean a worse outcome.

Time frame

24hours

Secondary outcomes

postoperative pain after 1, 3, 6, 12, 18, 48 hours

VAS (Visual analog scale) measured 1, 3, 6, 12, 18, 48 hours after operation * the unabbreviated scale title: The visual analog scale * the minimum and maximum values: 0, 10 * higher scores mean a worse outcome.

Time frame

1, 3, 6, 12, 18, 48 hours

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Chuncheon Sacred Heart Hospital

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: