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Active Not RecruitingNCT06916000

Assessment of PENG Block as a Part of Multimodal Analgesia Following Hip Surgeries.

Effect of Ultrasound Guided Pericapsular Nerve Group (PENG) Block on Perioperative Pain Management in Patients Undergoing Hip Arthroplasty

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Ain Shams University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

to study the effect of Pericapsular nerve group (PENG) block as a part of multimodal analgesia regimen for hip arthroplasties

Detailed description

PENG block is a novel block described by Giron-Arango in 2018 to anesthesize the anterior hip capsule as it is supplied by branches from femoral, obturator and accessory obturator nerves, sparing motor function is an additional significance So currently the block is used to reduce post operative opioid consumption, delay time rescue analgesia, facilitate positioning for spinal anesthesia for hip surgeries and to accelerate mobility and so hospital discharge saving this vulnerable group of patient from any hospital acquired pneumonia, decreasing hospital stays, and improving recovery times would provide valuable insights into its cost-effectiveness and long-term benefits for healthcare system Our primary outcome to be studied is pain assessment via Numer Rating Scale over 24 hours postoperatively, in addition to to secondary outcomes including the aforementioned advantages.

Conditions

Interventions

TypeNameDescription
DRUGPericapsular nerve group (PENG) blockAs a part of multimodal analgesia patients will receive 20 ml of 0.25% bupivcacaine according to the technique described by Giron-Arango. All patients will receive the same analgesic protocol, which included IV paracetamol 1000 mg BID and NSAIDs if no contra-indication; PO celecoxib 100 mg BID. Also if needed nalbuphine 5 mg IV will be given as bolus demand dose and when the NRS pain score was equal to or greater than 4 points.
OTHERPatients will receive only other multimodal analgesics including LCFN block via 10 ml of 0.25% bupivacaine.Patients will receive only other multimodal analgesics including LCFN block via 10 ml of 0.25% bupivacaine.

Timeline

Start date
2024-06-27
Primary completion
2025-06-01
Completion
2025-06-01
First posted
2025-04-08
Last updated
2025-04-08

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06916000. Inclusion in this directory is not an endorsement.