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Evaluation of analgesic effects of ultrasound-guided pericapsular nerve group (PENG) block combined with lateral femoral cutaneous nerve (LFCN) block in total hip replacement arthroplasty under spinal anesthesia

Evaluation of analgesic effects of ultrasound-guided pericapsular nerve group (PENG) block combined with lateral femoral cutaneous nerve (LFCN) block in total hip replacement arthroplasty under spinal anesthesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0007959
Enrollment
82
Registered
2022-12-05
Start date
2022-11-18
Completion date
Unknown
Last updated
2023-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others : No intervention group : Spinal anesthesia is performed without nerve block. Experimental group : 20ml of 0.5% Ropivacaine is injected into the anterior hip joint capsule and 5ml of 0.5% Ropiv

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Adults between 20 and 70 years of age - Patients undergoing THA - ASA physical status I,II : ex) Healthy adult without underlying disease (I), patient with systemic disease such as controlled hypertension or controlled diabetes, but can be controlled with medication or surgical treatment (II)

Exclusion criteria

Exclusion criteria: - ASA physical status III or higher - Pregnant - Patients with severe blood clotting disorders (last INR over 1.5 before surgery) - Patients with cerebrovascular disease - Systemic infection, patients with infection at the site of nerve block - Patients with chronic pain disorder or neurological disorder - Patients allergic to local anesthetics - Patients who did not understand this study and expressed their intention not to participate in the study - Patients who have communication problems or cannot express the severity of their pain

Design outcomes

Primary

MeasureTime frame
Maximum pain score measured at rest within 24 hours after surgery (NRS)

Secondary

MeasureTime frame
Maximum pain score (NRS) measured during motion within 24 hours after surgery;Maximum pain score at rest after surgery (NRS);Maximum pain score during motion after surgery (NRS);Cumulative opioid analgesic or acetaminophen usage after surgery;Satisfaction with pain control after surgery;Sleep satisfaction on the first day after surgery;Time of first administration of pain medication after surgery;Complications related to nerve block (nausea, vomiting, itching, dizziness, hypotension, hypopnea);Pre/post surgery Quality of recovery 15 questionnaire score;Motor weakness test - Quadriceps strength (knee extension test)

Countries

Korea, Republic of

Contacts

Public ContactKwan Young Hong

Samsung Medical Center

kwanyoung.hong@gmail.com+82-2-3410-0369

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026