FNB in ACL Recon Under GA

Status Not yet recruiting

Clinical Trial Summary

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

Clinical Trial Description

This study is a randomized controlled trial of 100 patients, who underwent history taking, physical examinations, x-rays, and MRI or ultrasonography, and were diagnosed with anterior cruciate ligament rupture from september 2023 to august 2028. The 100 patients will be assigned to Group I (with femoral nerve block) or Group II (without femoral nerve block) under double-blinded randomization. The randomization will be performed by an independent nurse using a computerized random sequence generator. The operators who participated in the procedure will be blinded to the participant's information. Both group will undergo general anesthesia for arthroscopic anterior cruciate ligament reconstruction. After anesthesia, sono-guided femoral nerve block will be performed. The injection for group1 is 20 mL ropivacaine and for groupII is 20 mL 0.9% saline. A visual analog scale (VAS) for pain will be recorded 1, 3, 6, 12, 18, 24, 36, 48 hours after the operation. VAS scores range from 0 to 10, with 0 being no pain and 10 being the most severe pain ever experienced. Injection with ultrasonography will be performed by a single anesthesiologist. 3 orthopedic surgeons will perform the surgery. ;

Study Design

Related Conditions & MeSH terms

Anterior Cruciate Ligament Rupture
Femoral Nerve Block
Rupture

Clinical Trial Details

NCT number	NCT06048848
Study type	Interventional
Source	Chuncheon Sacred Heart Hospital
Contact
Status	Not yet recruiting
Phase	N/A
Start date	September 18, 2023
Completion date	September 18, 2028

View Details

See also
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