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NCT05050487

Pericapsular Nerve Group Block Versus Lumber Erector Spinae Plane Block for Pain Management After Total Hip Arthroplasty

Status unknown NA Last updated 28 April 2022
What this trial tests

NA trial testing PENG block in Post Operative Pain, Chronic in 60 participants. Status unknown.

Timeline
30 June 2022
Primary endpoint
30 October 2023
30 December 2023

Quick facts

Lead sponsorAssiut University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment60
Start date30 June 2022
Primary completion30 October 2023
Estimated completion30 December 2023

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

Adults 18 to 80, any sex, with Post Operative Pain, Chronic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Pain is a major problem that has to be dealt with in case of hip fracture, as it presents an obstacle for examination, positioning for receiving neuroaxial anesthesia and postoperative mobility and physiotherapy. With the introduction of ultrasound in regional anesthesia and peripheral nerve blocks, regional analgesia float to the surface as a substitute for opioids with less side effects Lumbar erector spinae plane block has emerged as a reliable analgesic option for primary total hip arthroplasty (THA). In 2018, a new block was described, termed pericapsular nerve group block or PENG block, that selectively targets the articular branches of the femoral and obturator nerves while sparing their motor components

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of PENG block

Trials testing the same drug.

Other Assiut University trials

Trials by the same sponsor.

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Data sources for this page

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