Investigating the effect of adding metoclopramide to subcutaneous lidocaine on pain after lower abdominal surgery with general anesthesia

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20231228060548N1

Enrollment

Registered

2024-05-08

Start date

2023-03-21

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

Abdominal surgeries. Injuries to the abdomen, lower back, lumbar spine and pelvis

Interventions

Intervention 1: Intervention group: Group A (receiver of metoclopyramide and lidocaine). Intervention 2: Intervention group: Group B (lidocaine recipient).

Eligibility

Sex/Gender

All

Age

15 Years to 75 Years

Inclusion criteria

Inclusion criteria: Being 15-75 years old Signing a written informed consent form to enter the study 1 and 2 ASA Non-use of drugs and alcohol Elective surgery

Exclusion criteria

Exclusion criteria: Decreased level of consciousness Hemodynamic disorder Abnormal intraoperative bleeding Length of operation more than 4 hours

Design outcomes

Primary

Measure	Time frame
Pain after surgery. Timepoint: 1, 6, 12 and 24 hours after the operation. Method of measurement: VAS.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahnaz Narimani Zamanabadi

Islamic Azad University

mahnaznarimani@yahoo.com+98 21 2660 2642

Outcome results

None listed

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