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The comparison of efficacy between the suprainguinal fascia iliaca block and the modified pericapsular nerve group (PENG) block when combined with Transversalis fascia plane block for postoperative analgesia after total hip arthroplasty: A randomized control trial

The comparison of efficacy between the suprainguinal fascia iliaca block and the modified pericapsular nerve group (PENG) block when combined with Transversalis fascia plane block for postoperative analgesia after total hip arthroplasty: A randomized control trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210929001
Enrollment
60
Registered
2021-09-29
Start date
2021-10-14
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

osteoarthritis of hip patients undergoing total hip arthroplasty osteoarthritis of hip, total hip arthroplasty

Interventions

before start operation, the ultrasound-guided suprainguinal fascia iliaca block was done by 30 mL of 0.33% bupivacaine with epinephrine (1:200,000), and the ultrasound-guided transversalis fascia plan
SFIB group,PENG group

Sponsors

Chulalongkorn University research and innovation for society
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: osteoarthritis of hip patients undergoing total hip arthroplasty (American Society of Anesthesiologists class 1-3) with BMI 18-40 kg/m2

Exclusion criteria

Exclusion criteria: 1. deny to participate 2. Patients without ability to assess outcome eg. Dementia, Parkinson disease 3. History of allergy any drugs used in this study 4. Patients at risks of local anesthetic drug toxicity ( BMI<18, chronic liver disease, albumin level < 2.8 gm/dl) 5. Patients with contraindication of NSAIDs use 6. Chronic opioid use patients

Design outcomes

Primary

MeasureTime frame
postoperative fentanyl consumption 24 hours Fentanyl consumption in PCA

Secondary

MeasureTime frame
pain score of anterior hip at rest and during movement preoperative, PACU,6,12,24,48 hours numerical rating scale,perioperative intravenous fentanyl consumption intraoperative, PACU, 6, 24, 48 h postoperative fentanyl consumption in PCA,pain score of posterior hip at rest and during movement preoperative, PACU, 6, 12, 24, 48 h postoperative numerical rating scale ,pain score at surgical incision preoperative, PACU, 6, 12, 24, 48 h postoperative numerical rating scale,demand and delivery ratio of PCA fentanyl 6, 24, 48 h postoperative patient controlled analgesia machine,the comprehensive Silverman integrated approach (C-SIA) score 6, 24, 48 h postoperative patient controlled analgesia,the duration and incidence of loss of cutaneous sensory perception in the hip region until not different from inoperative hip cold and touch sensation,pain score of all hip at rest and during movement preoperative, PACU, 6, 12, 24, 48 h postoperative numerical rating scale,Time-up and go test preoperative, 48 h postoperative blinded assessor ,Quadriceps muscle strength test 0 and 90 degree preoperative, 12 and 24 h postoperative Hand held dynamometer,Length of stay the time from surgery until complete discharge criteria time,patient satisfaction before discharge numerical rating scale,nausea/vomiting 6, 12, 24, 48 h postoperative numerical rating scale,dizziness 6, 12, 24, 48 h postoperative numerical rating scale ,sleep disturbance 6, 12, 24, 48 h postoperative yes/no

Countries

Thailand

Contacts

Public ContactChutikant Vichhainarong

King Chulalongkorn Memorial Hospital

braink5@docchula.com0919359396

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026