Skip to content

The role of zinc supplementation in neonatal sepsis

The effect of zinc supplementation on the treatment of neonatal sepsis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200810048347N1
Enrollment
50
Registered
2020-12-11
Start date
2018-03-21
Completion date
Unknown
Last updated
2021-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neonatal sepsis. Other sepsis

Interventions

Intervention 1: Intervention group: the intervention group received 1 mg/kg zinc gluconate manufactured by Alhawi (1 mg/ml) orally, via a nasogastric or orogastric tube, twice a day for one week. Int

Sponsors

Technology and Research Vice-chancellery, Hormozgan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Days to 28 Days

Inclusion criteria

Inclusion criteria: Presence of at least 2 clinical signs of sepsis including pallor or generalized jaundice, cardiovascular manifestations (tachy- or bradycardia, poor perfusion, or shock), change in body temperature (hypo- or hyperthermia), respiratory manifestations (grunting, intercostal retraction, apnea, or cyanosis), neurologic manifestations (hypotonia, lethargy, irritability, or seizure), gastrointestinal symptoms (abdominal distension, hepatosplenomegaly) CRP >5 mg/ml Presence of at least 1 positive serum parameter based on Fanarrof (book) including WBC 25000 at birth or WBC>30000 12-24 hours after birth or WBC>21000 on the second day of birth or the following days, absolute neutrophil count (ANC) 37 weeks Age <28 days Informed consent of the parents

Exclusion criteria

Exclusion criteria: Important congenital anomalies such as trisomies Hypoxic ischemic encephalopathy Intracranial hemorrhage Respiratory distress syndrome Inborn errors of metabolism Candidiasis

Design outcomes

Primary

MeasureTime frame
Mortality. Timepoint: At the end of the study. Method of measurement: Based on patient's medical chart.

Secondary

MeasureTime frame
Time to improvement of clinical symptoms. Timepoint: At the end of the study. Method of measurement: Daily clinical examination.;Hospital length of stay. Timepoint: At the end of the study. Method of measurement: Based on the patient's clinical charts.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSimin Yazdi

Bandar Abbas Pediatric Hospital

siminyazdi.hums@gmail.com+98 76 3366 6242

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026