Effect of Erector Spine Block and External Oblique Intercostal Block with Ultrasonography Guided to pain control

Comparison of Erector Spine Block and External Oblique Intercostal Block with Ultrasonography Guided to pain control after laparoscopic cholecystectomy surgery a clinical trial

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230518058225N9

Enrollment

Registered

2025-02-22

Start date

2025-03-10

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Pain. Pain, not elsewhere classified

Interventions

Intervention 1: Intervention group 1: In the erector spinae block group, the patient will be placed in the lateral position, then by examining the injection site and monitoring and necessary preparati

Eligibility

Sex/Gender

All

Age

20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patient candidates for laparoscopic cholecystectomy surgery The age range from 20 to 60 years

Exclusion criteria

Exclusion criteria: Severe pulmonary disease Neurological disorders

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: at 0, 2, 6, 12, 24 hours after surgery. Method of measurement: Numerical pain rating scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNafiseh Tavakoli

Iran University of Medical Sciences

ntvk1356@gmail.com+98 21 6435 2222

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026