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The efficacy of quadratus lumborum block in a patients with hip arthroplasty

The analgesic efficacy of Quadratus lumborum block after hip arthroplasty: a prospective randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002227
Enrollment
62
Registered
2017-02-14
Start date
2017-02-20
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Procedure/Surgery : Epidural anesthesia is performed in all patients. And they are randomly assigned to two groups. In the quadratus lumborum block (QLB) group, the patients receive intravenous patien
ropivacaine 20ml with 1:200000 epinephrine, ipsilateral one side). In the control group, the patients only receive Intravenous PCA without QLB. The pain score and opioid consumption will be check to
ropivacaine 20ml with 1:200000 epinephrine was injected. Ultrasound: (WS80A, Samsung Medicine, Korea) Local anesthetic: QLB - 0.375&#37
ropivacaine 20ml with 1:200000 epinephrine, (Naropin®, AstraZeneca, UK) PCA regimen: no continuous infusion, total fentanyl 20 mcg/kg, total volume 100 ml, bolus fentanyl 0.5 mcg/kg , lock time 7 mi

Sponsors

The Catholic University of Korea, Daejeon St. Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: American society of anesthesiology (ASA) 1, 2, 3 Age: 19-70 yrs Patients undergoing hip arthroplasty

Exclusion criteria

Exclusion criteria: Clinically significant coagulopathy Infection at the injection site Allergy to local anesthetics Severe cardiopulmonary disease(=American society of anesthesiology (ASA) physical status 4) Body mass index > 35 Diabetic or other neuropathies Patients receiving opioids for chronic analgesic therapy Patients who have refused intravenous patient controlled analgesia (PCA) Inability to comprehend visual analogue scale (VAS) score and patient controlled analgesia (PCA) device Patient who does not want to receive quadratus lumborum block Patients who want to receive a quadratus lumborum block

Design outcomes

Primary

MeasureTime frame
Amount of opioid consumption

Secondary

MeasureTime frame
Postoperative pain score (visual analogue scale, VAS)

Countries

Korea, Republic of

Contacts

Public ContactSeunguk Bang

The Catholic University of Korea, Daejeon St. Mary's Hospital

seungukb@naver.com+82-42-220-9046

Outcome results

None listed

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