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Adding pericapsular nerve group (PENG) block for postoperative pain relief following elderly hip fracture surgery: A prospective randomized controlled trial.

Adding pericapsular nerve group (PENG) block for postoperative pain relief following elderly hip fracture surgery: A prospective randomized controlled trial.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220622003
Enrollment
60
Registered
2022-06-22
Start date
2021-10-01
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

Hip fracture is the main cause of impairment and death, especially among the elderly. At present, elderly hip fracture number is rising in line with rising elderly population. It is estimated that there were 1.66 million elderly hip fractures in 1990, and the figure is expected to rise to 6.26 million in 2050. Several studies reveal that prompt hip surgery within 48 hours significantly reduced pain, surgery complications, and deaths. Cochrane study found that regional anesthesia could reduce com

Interventions

FICB: 0.25% bupivacaine 20 ml PENG:0.25% bupivacaine 20 ml , FICB: 0.33% bupivacaine 30 ml
FICB+PENG ,FICB

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
64 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. 65+ years old 2.ASA classification I-III

Exclusion criteria

Exclusion criteria: Alzheimer patients, incapable of pain level description, allergic history of bupivacaine, paracetamol, morphine, prohibition against spinal cord anesthesia and FICB and/or PENG block, pre-existing ailments such as heart failure, irregular acute heart pain, chronic obstructive lung disease, cerebrovascular disease and terminal chronic kidney failure

Design outcomes

Primary

MeasureTime frame
Postoperative pain score 12 hours Numerical rating scale

Secondary

MeasureTime frame
Postoperative pain score 24 hours Numerical rating scale,Postoperative pain score 48 hours Numerical rating scale,Morphine consumption 48 hours Total morphine requirement,Time to first sitting without pain within 48 hours after end of the intervention Time,Time to first morphine requirement within 48 hours after end of the intervention Time,Complications such as nausea, vomiting, dizziness, respiratory depression within 48 hours after end of the intervention questionnaire interview

Countries

Thailand

Contacts

Public ContactLuckapa Nuthep

Buddhachinaraj hospital

jjpy2555@gmail.com055270300

Outcome results

None listed

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