PENG Block vs ESPB in Elderly Undergoing Hip Surgeries
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: PENG block, ESPB.
- Who it may be relevant to
- Registry conditions: Anesthesia for Hip Surgery. Basic parameters: from 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Comparison Between the Ultrasound Guided Pericapsular Nerve Group Block and Erector Spinae Plane Block on Motor Power Postoperative in Elderly Patients Undergoing Total Hip Replacement Surgeries; A Randomized Controlled Trial
Overview
To our knowledge, the comparison between the ultrasound-guided lumbar erector spinae plane block and the pericapsular nerve group block has not been investigated before in previous literature.
Interventions
- Procedure PENG block
Group LESBP: 28 patients will receive single shot LESPB after spinal induction. Group PENG: 28 patients will receive single shot PENG after spinal induction. - Procedure ESPB
Group LESBP: 28 patients will receive single shot LESPB after spinal induction. Group PENG: 28 patients will receive single shot PENG after spinal induction.
Primary outcome measures
- Motor power [Time frame: 24 hours postoperative]
Eligibility criteria
Inclusion criteria
- Both genders Type of surgery; unilateral elective total hip replacement. Physical status ASA I, II Age more than or equal 65 Years. Body mass index (BMI): > 20 kg/m2 and < 35 kg/m2.
Exclusion criteria
- Patient refusal. Patients with known sensitivity or contraindication to drugs used in the study (local anesthetics \& opioids).
History of psychological disorders and/or chronic pain. Pre- existing peripheral neuropathies Coagulopathy. Infection of the skin at the site of needle puncture area.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06993376 · N22-2023/MD