Clarifying confusion: the confusion assessment method. A new method for detection of delirium.
S K Inouye, C H van Dyck, C A Alessi...
https://pubmed.ncbi.nlm.nih.gov/2240918Actively Recruiting
Led by Fayoum University Hospital · Updated on 2026-03-03
80
Participants Needed
1
Research Sites
4 weeks
Total Duration
This research aims to compare two types of nerve blocks, sacral erector spinae plane block (S-ESPB) and pericapsular nerve group (PENG) block, for pain relief after hip hemiarthroplasty in patients aged 50 to 90 years with femoral neck fractures. These blocks are being studied because they may provide effective pain control while preserving muscle strength, aligning with recovery protocols that emphasize pain management, limited opioid use, and early movement to reduce complications. Participants will be randomly assigned to receive either the sacral ESPB or the PENG block after spinal anesthesia and before surgery begins. The sacral ESPB is performed with the patient lying on their side, while the PENG block is done with the patient lying on their back. Both blocks use ultrasound guidance to accurately place local anesthetic near targeted nerves, with strict safety measures to avoid toxicity and adverse events. All patients will receive standard spinal anesthesia and a uniform pain medication plan including paracetamol, NSAIDs, and opioids if needed. During the study, patients will be monitored for pain levels using a numeric rating scale at rest and during movement at multiple times within 24 hours after surgery. Other measures include opioid use, timing of first rescue pain medication, ability to participate in physiotherapy, delirium signs, motor function, side effects linked to opioids, and hospital stay length. Safety monitoring will check for block-related complications and adverse reactions. Total participation covers the surgery day and up to 30 days of follow-up for hospital discharge assessment.
CONDITIONS
Sacral ESPB vs. PENG Block for Hip Hemiarthroplasty Analgesia
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants receive spinal anesthesia followed by either a sacral erector spinae plane block or a PENG block before surgery to manage pain during hip hemiarthroplasty.
1 visit (in-person, on surgery day)
Duration - Up to 30 days post-surgery
Participants are monitored for pain, opioid consumption, motor block, side effects, and adverse events during the first 24 hours after surgery, with delirium assessments twice daily for 3 days and hospital stay up to 30 days.
Multiple visits for up to 30 days including assessments at 2, 4, 6, 8, 12, 18, 24 hours postoperatively and twice daily delirium assessments for 3 days
Total: 1 location
1
Fayoum University hospita
El Fayoum Qesm, Faiyum Governorate, Egypt, 63514
Actively Recruiting
S
Samar Ahmed Ramadan
M
Mohamed Ahmed Hamed
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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