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

Phase 3
Conditions
Abdominal surgeries.
Injuries to the abdomen, lower back, lumbar spine and pelvis
Registration Number
IRCT20231228060548N1
Lead Sponsor
Islamic Azad University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
58
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

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

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain after surgery. Timepoint: 1, 6, 12 and 24 hours after the operation. Method of measurement: VAS.
Secondary Outcome Measures
NameTimeMethod
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