Skip to content

the effect of magnesium on pain relief

the effect of administration of intravenous magnesium on pain relief in patients after major abdominal surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210214050359N1
Enrollment
84
Registered
2021-08-24
Start date
2021-09-11
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

major abdominal surgery. personal history of major abdominal surgery

Interventions

Intervention 1: Intervention group: Administration of 100 mg per kg of body weight of 20% magnesium sulfate solution for a total of 24 hours in equal parts per liter of isotonic saline solution prescr

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Candidates for major abdominal surgery Candidates for icu after abdominal surgery

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArash Peivandi Yazdi

Mashhad University of Medical Sciences

peivandia@mums.ac.ir+98 51 3854 3031

Outcome results

None listed

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