Assessment of the efficacy of ultrasound guided erector spinae plane block for postoperative analgesia in thoracolumbar spinal surgeries

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

PACTR

Registry ID

PACTR201910691333405

Enrollment

Registered

2019-10-17

Start date

2019-09-01

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

Anaesthesia

Interventions

Control

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: ASA 1-3 patients scheduled for lower thoracic or lumbar spinal surgery Age 18-65 years Sex: Both male and female

Exclusion criteria

Exclusion criteria: Patient with chronic pain syndrome Patients on long term opioids. History of allergy to local anaesthetics Recurrent back surgeries Chronic Kidney disease

Design outcomes

Primary

Measure	Time frame
Post operative morphine consumption in milligrams for the first 24 hours after surgery, compared to the consumption of the control group to assess if the intervention will reduce the opioid needs in thorasic and lumbar spine surgery.Pain will be assessed using the visual analogue scale.	—

Secondary

Measure	Time frame
Visual Analogue Scale will be assessed directly postoperative and then every 6 hours till the end of the first 24 hours after surgery. ;First analgesic request	—

Countries

Egypt

Contacts

Public ContactMostafa Abdelrahman

Suez Canal university

m.mahmoud.scuh@gmail.com+201098984116

Outcome results

None listed

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