The Postoperative Analgesic Effect of Lumbar Erector Spinae Plane Block versus Pericapsular Nerve Group Block in Patients Undergoing Hip Surgeries

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

PACTR

Registry ID

PACTR202409764079235

Enrollment

Registered

2024-09-06

Start date

2023-03-01

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

Anaesthesia

Interventions

Pericapsular nerve group block

Erector spinae plane block

Control group

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who will undergo hip surgery. Patients of either sex. Patients above the age of 18. Patients with the American Society of Anesthesiologists (ASA) classes I and II.

Exclusion criteria

Exclusion criteria: Patient refusal for regional anesthesia. History of local anesthetic allergy, bleeding disorder or anticoagulant therapy. local-site infection. Clinical significant neurological disease. ASA Clases III and IV.

Design outcomes

Primary

Measure	Time frame
The numerical rating scale NRS at the time before and 30 min after the blockade (by passive internal rotation of the fractured lower limb to neutral position from its typical external rotation deformity), and at 3, 6, 12, 18, 24 and 48 hours postoperative of both resting and dynamic pain.	—

Secondary

Measure	Time frame
The strength of the quadriceps, the total morphine consumption, the first time of postoperative out-of-bed mobilization and any complications will be recorded.	—

Countries

Egypt

Contacts

Public ContactIslam ElDesoky

Department of Anesthesiology Intensive Care and Pain Management Faculty of Medicine Menoufia University 32511 Shebin ElKom Menoufia Egypt.

islamdesoky@gmail.com+201092447887

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026