Lumbar erector spinae plane block versus iliopsoas plane block for hip arthroplasty analgesia

Efficacy of the Lumbar erector spinae plane block on the quality of analgesia after hip arthroplasty; a prospective randomized comparative study with iliopsoas plane block

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR202301914053306

Enrollment

Registered

2023-01-26

Start date

2023-01-07

Completion date

Unknown

Last updated

2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anaesthesia

Interventions

Lumbar erector spinae plane block

Iliopsoas plane block

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: either sex, aging > 18 , ASA I–III undergoing hip arthroplasty under spinal anesthesia

Exclusion criteria

Exclusion criteria: * Patients who refuse to participate, * Have a history of bleeding disorder, *Receiving anticoagulant medications, * Polytrauma patients * Patients who had chronic pain or had received opioid analgesic in the preceeding two weeks, * Patients with an infection at the sites of injections, and * Patients who are unable to communicate.

Design outcomes

Primary

Measure	Time frame
The cumulative PCA morphine consumption after surgery	—

Secondary

Measure	Time frame
1. Pain scores at rest and on movement evaluated by VAS score at PACU,1, 2, 4, 6, 12 and 24h after surgery. 2. Time to first rescue analgesia (the duration of postoperative analgesia). 3. Quadriceps strength will be assessed using manual muscle testing grades (MMT grades) (0–5; 0: no muscle contraction, 5: can bear full resistance). 4. Adverse effects; sedation, nausea, vomiting, pruritus and needle trauma.	—

Measure

Time frame

1. Pain scores at rest and on movement evaluated by VAS score at PACU,1, 2, 4, 6, 12 and 24h after surgery. 2. Time to first rescue analgesia (the duration of postoperative analgesia). 3. Quadriceps strength will be assessed using manual muscle testing grades (MMT grades) (0–5; 0: no muscle contraction, 5: can bear full resistance). 4. Adverse effects; sedation, nausea, vomiting, pruritus and needle trauma.

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Countries

Egypt

Contacts

Public ContactSherin Bakrey

Lecturer

Rosh_2000@yahoo.com00201022544897

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Feb 4, 2026