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the effect of magnesium on pain relief

Phase 3
Conditions
major abdominal surgery.
personal history of major abdominal surgery
z92.4
Registration Number
IRCT20210214050359N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
84
Inclusion Criteria

Candidates for major abdominal surgery
Candidates for icu after abdominal surgery

Exclusion Criteria

heart failure
renal failure
hepatic failure
sensitivity to magnesium sulfate
poisoning to magnesium sulfate
drug abuse
neuromuscular disease
Dissatisfaction
Lack of cooperation

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: every 3 hours. Method of measurement: After the necessary training to the patient, pain intensity is measured every 3 hours for 24 hours based on the unit of numerical pain rating scale.;Level of Prescription morphin. Timepoint: every 3 hours. Method of measurement: The total morphine injected in the first 24 hours of entering the ICU to reduce the severity of pain is calculated to be less than 3.;Level of serum magnesium sulfate. Timepoint: Upon arrival and after 24 hours. Method of measurement: Serum magnesium sulfate levels are measured by blood sample at the time of entry into the ICU and after 24 hours.
Secondary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: every 3 hours. Method of measurement: Sphygmomanometer.;Respiratory rate. Timepoint: every 3 hour. Method of measurement: counting respiratory rate in 1 minute.;Pulse rate. Timepoint: every 3 hours. Method of measurement: pulseoxymetery.;O2 saturation. Timepoint: every 3 hours. Method of measurement: pulseoxymetery.
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