Erector spinae plan block

Ultrasound-guided erector spinae block in patients undergoing laparoscopic bariatric surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201706002388985

Enrollment

Registered

2017-06-28

Start date

2017-05-01

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

Postoperative pain Anaesthesia

Interventions

Control group

ESPB Group

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: ages 18-65 yrs; body mass index (BMI) of more than 40 kg/m2; ASA physical status II-III undergoing laparoscopic bariatric surgery

Exclusion criteria

Exclusion criteria: allergy to any of the study drugs: coagulation disorders; psychiatric or uncooperative patients; patients with hepatic or renal dysfunction; Patients with history of uncontrolled respiratory / cardiovascular morbidity; Pregnant ladies

Design outcomes

Primary

Measure	Time frame
Postoperative VAS	—

Secondary

Measure	Time frame
consumption of intraoperative fentanyl;postoperative rescue analgesia	—

Countries

Egypt

Contacts

Public ContactMohamed;Mohamed Mohye Eldin;Mohye Eldin

Lecturer of anesthesia and ICU. Faculty of Medicine, Tanta University;Lecturer of Anesthesia and ICU, Faculty of Medicine, Tanta University

Mohd_yazed75@yahoo.com;Mohd_yazed75@yahoo.com01120014472;01120014472

Outcome results

None listed

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