Ultrasound Guided lumbar erector spinae plane block as a Supplement to General Anesthesia for postoperative pain management in orthopedic surgery: A Comparison Between different Drug Combinations.

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

PACTR

Registry ID

PACTR202001840074546

Enrollment

Registered

2020-01-13

Start date

2019-12-23

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

erector spinae block

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Anesthesiologists physical status class I, II, III undergoing elective surgeries performed under general anesthesia

Exclusion criteria

Exclusion criteria: with spine deformity, infection at the block site, drug allergy, renal disease coagulation disorders

Design outcomes

Primary

Measure	Time frame
the amount of analgesics used in the first 24 postoperative hours.	—

Secondary

Measure	Time frame
intraoperative fentanyle consumption, time to the first call for analgesia starting from the administration of the ESPB block till the patient asks for analgesia postoperatively. The severity of both nausea and sedation was assessed by patients on a 4-point scale (none, mild, moderate, and severe). all the patients were also evaluated for any complications	—

Countries

Egypt

Contacts

Public Contactnoha afify

lecturer in anesthesiology department

nohaafify2014@gmail.com01069113014

Outcome results

None listed

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