Comparison of the effect of norepinephrine with and without dobutamine on mortality and morbidity of children with septic shock

Phase 2

Recruiting

• Conditions: Septic shock.; Postprocedural septic shock; T81.12

• Registration Number: IRCT20101220005426N13
• Lead Sponsor: Kerman University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Children in the age group of 2 to 14 years
Children with septic shock
They need to transfer to the intensive care unit

Exclusion Criteria

Children with organ failure
The patient's lack of consent, or if the patient is unable to answer, the patient's guardian's lack of consent
The presence of heart failure, kidney and diabetes

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hemodynamic and blood supply findings (CO-MAP-HR). Timepoint: Measuring CO-MAP-HR at the beginning of the study (before the intervention) and then every hour until the end of the study. Method of measurement: Ecocardiography.;Vasopressor dependence days. Timepoint: The number of days that patients receive vasopressor. Method of measurement: Check list.;Urinary tract. Timepoint: At the beginning of the study and then every 6 hours until the end of the study. Method of measurement: Check list.;Duration of hospitalization in the intensive care unit. Timepoint: At the beginning of the study and then daily until the end of hospitalization in the relevant department. Method of measurement: Check list.;Serum lactate level. Timepoint: At the beginning of the study, then daily until the end of the study. Method of measurement: AutoAnalyzer.;Electrolytes (urea, creatinine). Timepoint: At the beginning of the study, then daily until the end of the study. Method of measurement: AutoAnalyzer.