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Effect of magnesium sulfate on blood infection

Evaluation of the effect of magnesium sulfate on lactate clearance in sepsis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180410039254N1
Enrollment
50
Registered
2018-07-11
Start date
2018-06-22
Completion date
Unknown
Last updated
2018-09-11

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

Conditions

Sepsis. Gram-negative sepsis, unspecified

Interventions

Intervention 1: Intervention group: 25 patients will be received magnesium sulfate (2 g magnesium sulfate in 50 ml of normal saline over one hour) as intravenous infusion. Infusion of magnesium sulfat

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Critically ill adult patients (18-65 years old) admitted to ICU with diagnosis of sepsis will be included.

Exclusion criteria

Exclusion criteria: Exclusion criteria: Patients with hypermagnesemia (serum magnesium level> 3.5 mg/dL, hypomagnesemia (serum magnesium level<1.5 mg/dL), renal failure (GFR <30 ml/min /1.73 m2), moderate to severe hepatic insufficiency (child pugh score B, C), seizure , chronic alcohol consumption, malignancy, MAP <65 mm Hg resistant to vasopressors, diabetic ketoacidosis and pregnant women will be excluded.

Design outcomes

Primary

MeasureTime frame
Lactate clearance. Timepoint: At the beginning of the study (before the intervention) and then every 6 hours on the day 0 - Day 1 - Day 2. Method of measurement: By spectrophotometry and Pars-Azmoon kit in mg/dl.;Serum magnesium level. Timepoint: At the beginning of the study (before the intervention) and then every 6 hours on the day 0 - Day 1 - Day 2. Method of measurement: By spectrophotometry and Pars-Azmoon kit in mg/dl.;Intracellular magnesium concentration (RBC magnesium level). Timepoint: At the beginning of the study (before the intervention) and then every 6 hours on the day 0 - Day 1 - Day 2. Method of measurement: By spectrophotometry and Pars-Azmoon kit in mg/dl.

Secondary

MeasureTime frame
SOFA score (Sepsis-related organ failure assessment score). Timepoint: At the beginning of the study (before the intervention), then daily on day 0 - day 1- day 2. Method of measurement: Based on the SOFA score scale.;APACHE II score ( Acute Physiologic And Chronic Health Evaluation ). Timepoint: At the beginning of the study (before the intervention), then daily on day 0 - day 1- day 2. Method of measurement: Based on the APACHE-II score scale.;Duration of intensive care unit stay. Timepoint: Daily. Method of measurement: Count the number of hospitalization days in the intensive care unit.;Mortality. Timepoint: Daily. Method of measurement: Count the number of dead patients.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Khalili

Tehran University of Medical Sciences

khalilih@tums.ac.ir+98 21 6658 1598

Outcome results

None listed

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