Lower Vs. Standard Insulin-Dextrose Doses for Treating Mild to Moderate Hyperkalemia in the Emergency Department (IDK+)

NCT06724991 NA NOT_YET_RECRUITING

This clinical trial aims to evaluate the safety and efficacy of a lower dose insulin compared to the conventional dose for treating mild to moderate hyperkalemia, a condition characterized by elevated serum potassium levels below 6.4 mmol/L. The study focuses on adult patients in the emergency department. The primary objective is to determine whether the efficacy of lower doses of insulin and dextrose is non-inferior to conventional doses in reducing serum potassium levels in patients with mild to moderate hyperkalemia. The research compares two regimens: 5 units of insulin with 25 mL of dextrose 50% versus 10 units of insulin with 50 mL of dextrose 50%, assessing the mean reduction in serum potassium levels, the incidence of hypoglycemia, and the risk of extravasation injury. Participants will be monitored in the emergency department for 6 hours. Serum potassium levels will be measured at 1, 2, 4, and 6 hours post-intervention, while blood glucose levels will be monitored at 30, 60, 90, 120, 240, 300, and 360 minutes post-intervention.

Details

Lead sponsor	University of Malaya
Phase	NA
Status	NOT_YET_RECRUITING
Enrolment	50
Start date	Wed Jan 01 2025 00:00:00 GMT+0000 (Coordinated Universal Time)
Completion	Tue Jun 01 2027 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

• Hyperkalemia

Interventions

• Lower Dose Therapy
• Conventional Dose Therapy

Countries

Malaysia