Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age1-5
SponsorTanta University
About this trial
Pediatric population who suffered from sepsis due to perforated viscus will receive fluid resuscitation guided by either central venous pressure or guided by IVC collapsibility index.
The method of guidance of fluid therapy will be applied pre, intra, and postoperatively.
Primary outcome will be the length of hospital stays, while the secondary outcomes will be the incidence of complications and the length of PICU stays
Eligibility criteria
Qualifiers
Pediatric patients aged 1 to 5 years presented with septic shock due to perforated viscus according to definition of the American College of Critical Care Medicine and International Pediatric Sepsis Consensus.
Disqualifiers
Refusal of the parents to participate in the study
Obesity
Congenital heart diseases
Severe arrythmias
Trial design
Treatments tested in this trial
- Central venous catheter
- IVC collapsibility index
Treatment groups
50 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov