drugset / Trial / NCT05257031

Efficacy and Safety of SmofKabiven Extra Nitrogen for Parenteral Nutrition in Patients Receiving Intensive Care

NCT05257031 ↗

Phase 3 Completed 56 enrolled Fresenius Kabi
NaSingle-groupOpen-labelSupportive care

Summary

The aim of this clinical trial is to assess the efficacy and safety of the investigational product SmofKabiven extra Nitrogen in patients requiring parenteral nutrition (PN) to achieve the target protein dose. The cumulative target protein dose is 6.2 g per kg of body weight (BW) over the five study treatment days, with 1.0 g/kg BW on Study Day 1 and 1.3 g/kg BW per day on Study Days 2-5; the target caloric intake is 15 kcal/kg BW on Study Day 1 and 20 kcal/kg BW/day on Study Days 2-5, following the recommendation of the ESPEN guideline on clinical nutrition in the intensive care unit 2019 regarding a slow-ramp up of calories during the first week of critical illness.

Timeline

Start
2022-02-12
Primary completion
2022-09-11
Completion
2023-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject SmofKabiven extra Nitrogen Other / unclassified — Other

Indications

No indication recorded.