Combined adductor canal (ACB) and sacral erector spinae plane (S-ESP) blocks for total knee arthroplasty pain in hemophilic arthropathy.
Francesco Marrone, Pierfrancesco Fusco, Saverio Paventi...
https://pubmed.ncbi.nlm.nih.gov/39600436Actively Recruiting
Led by San Giovanni di Dio Hospital · Updated on 2025-08-28
126
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are evaluating the effectiveness and recovery outcomes of two combinations of locoregional anesthesia in adults over 18 years old undergoing unilateral total knee arthroplasty (TKA) under spinal anesthesia. The study compares the combination of adductor canal block (ACB) with sacral erector spinae plane (ESP) block to ACB combined with iPACK block. It aims to determine whether the ACB plus sacral ESP block provides effective pain relief and postoperative recovery. Participants receive spinal anesthesia and multimodal postoperative pain management, including paracetamol and rescue tramadol. The sacral ESP block is administered at the S2 level using ultrasound guidance and ropivacaine, while ACB and iPACK blocks follow standard protocols. Patients already receiving ACB plus sacral ESP block as part of their care will be observed for up to 48 hours after surgery. During the study, researchers will monitor recovery quality using the QoR-15 score at 24 hours, measure pain levels at rest and during movement over 48 hours, track time to first mobilization, analgesic consumption, and patient satisfaction. They will also watch for any complications related to the nerve blocks. The study lasts up to 30 months, and all data collection respects patient privacy and ethical standards.
CONDITIONS
The Sacral Erector Spinae Plane Block in Total Knee Arthroplasty
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Hospitalization longer than 24 hours
Participants undergo unilateral total knee arthroplasty under spinal anesthesia with regional nerve blocks for postoperative pain control.
1 hospitalization period including surgery
Duration - 48 hours post-surgery
Participants are observed for recovery quality, pain levels, analgesic use, and time to mobilization during the first 48 hours after surgery.
Assessments during hospitalization up to 48 hours
Total: 1 location
1
San Giovanni Crotone Hospital
Crotone, Italy
Actively Recruiting
T
Tommaso Sorrentino, Anesthesiology
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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