PENG for perioperative analgesia in hip fracture surgery

Continuous pericapsular nerve group block for perioperative analgesia in hip fracture surgery, a prospective randomized study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR202002906402947

Enrollment

Registered

2020-02-25

Start date

2020-03-01

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Orthopaedics Anaesthesia

Interventions

PENG group

Control group

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: patients scheduled for hip surgery

Exclusion criteria

Exclusion criteria: Patients with contraindication to spinal anesthesia (thrombocytopenia (less than 100), INR more than 1.5, valvular stenotic lesions), refusing enrollment, and difficulty to express pain scores will be excluded from the study.

Design outcomes

Primary

Measure	Time frame
Morphine consumption in milligrams	—

Secondary

Measure	Time frame
perioperative pain scores;Duration of sensory block;quadratus muscle weakness	—

Countries

Egypt

Contacts

Public ContactAlrefaey Alreafey

Lecturer

refa3ey2@yahoo.com+201064203475

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026