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The effect of magnesium sulfate loading dose in treatment of diabetic ketoacidosis

Phase 3
Conditions
Diabetic ketoacidosis.
Diabetes mellitus due to underlying condition with ketoacidosis
E08.1
Registration Number
IRCT20220928056051N3
Lead Sponsor
Oroumia University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
50
Inclusion Criteria

Patients with diabetic ketoacidosis
Age between 14-65 years

Exclusion Criteria

Hypermagnesemia (magnesium more than 3 mg/dL)
Hypomagnesemia (magnesium less than 1.5 mg/dL)
Having clinical symptoms of hypermagnesemia including neuromuscular symptoms (loss of deep tendon reflexes, muscle paralysis, apnea) and cardiovascular symptoms
Severe renal failure (GFR < 30 ml/min/1.73 m2)
Patients with drug poisoning
Pregnancy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The total dose of prescribed insulin until the patient exits from acute phase of diabetic ketoacidosis. Timepoint: Daily until the third day after the intervention. Method of measurement: Vial.;The total dose of prescribed potassium until the patient exits from acute phase of diabetic ketoacidosis. Timepoint: Daily until the third day after the intervention. Method of measurement: Vial.;The length of time it will take time to convert insulin administration from IV to subcutaneous form. Timepoint: Until the third day after the intervention. Method of measurement: Clock.
Secondary Outcome Measures
NameTimeMethod
Prolonged time for patient recovery from acute phase of diabetic ketoacidosis. Timepoint: Until the third day after the intervention. Method of measurement: Clock.;Serum magnesium. Timepoint: Before and daily until the third day after the intervention. Method of measurement: Blood test.;Fasting blood sugar. Timepoint: Before and daily until the third day after the intervention. Method of measurement: Blood test.
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