About this trial
The aim is to demonstrate that lumbar ESP block provides more effective postoperative analgesia than PENG block in geriatric patients with hip fractures, and reduces postoperative opioid consumption more than PENG block
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
patients with hip fractures
over 65 years old
Disqualifiers
long-term surgery
Patients who do not want regional anesthesia
bleeding disorder disease
wound in the operation area
Trial design
Parallel
Treatments tested in this trial
Postoperative pain assessment of patients who underwent block
Procedure/SurgeryPostoperative pain assessment of patients who underwent block
Treatment groups
Trial outcomes
Primary outcomes
postoperative pain
To evaluate postoperative pain after two different block applications in patients undergoing hip fracture surgery.Evaluation of patients' postoperative 30th minute, 2nd hour, 6th hour, 12th hour and 24th hour verbal analog scores.To examine the total fentanyl consumption, acetaminophen consumption, and nonsteroidal anti-inflammatory drug consumption of patients in the postoperative 24 hours.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: