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Role of Zinc in Neonatal sepsis: A double blinded, randomized, placebo controlled trial

Phase 1
Registration Number
CTRI/2010/091/001061
Lead Sponsor
il
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
614
Inclusion Criteria

Inborn and Outborn neonates >32 weeks (By Ballard scoring) with Probable Neonatal Sepsis* will be included in this study.
*According to the guidelines formulated by the National Neonatology Forum of India based on the duly approved tenth revision of the International Classification of Diseases (ICD) by the WHO, in an infant having a clinical picture suggestive of sepsis, the presence of any one of the following criteria is enough to suspect the diagnosis of Bacterial Infection:
1)Existence of any of the predisposing factors like Premature Rupture of membranes (PROM), foul smelling liquor, Amnionitis or Funisitis, Gastric Polymorphs of more than 5/HPF.
2)Positive sepsis screen i.e. presence of atleast two of the following five parameters, namely, total leucocyte count < 5000/mm3, Low absolute neutrophil count (as per standard charts), Bands to Total neutrophil ratio (IT Ratio) of >0.2, C-Reactive Protein > 1mg/dl, Micro ESR > 15mm in first hour on any day of life/ age in days+3

Exclusion Criteria

The following categories of babies will be excluded from the trial:Preterm neonates < 32 weeks
Neonates with Congenital Malformations
Neonates with NEC

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Decrease in MortalityTimepoint: 10 days
Secondary Outcome Measures
NameTimeMethod
1)Duration of hospital stay (in hours)<br>2)Requirement of higher lines of antibiotic therapy (based on clinical assessment and culture reports)<br>Timepoint: 10 days
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