Skip to content

Examination of the Effect of Antibiotics on Inflammatory Factors in Neonates

Examination of proinflammatory and inflammatory cytokines in full-term neonates suspected of sepsis prior to and 12 hours after antibiotic therapy (pilot study)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201504289568N13
Enrollment
40
Registered
2015-06-02
Start date
2015-05-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Bacterial sepsis of newborn. Bacterial sepsis of newborn

Interventions

Antibiotic therapy with ampicilin+amikacin or rarely vancomycin+meropenem.
Treatment - Drugs
Antibiotic therapy with ampicilin+amikacin or rarely vancomycin+meropenem

Sponsors

Shahed university
Lead Sponsor
Tehran University of Medical Sciences
Collaborator

Eligibility

Sex/Gender
All
Age
No minimum to 28 Days

Inclusion criteria

Inclusion criteria: Inclusion criteria: All healthy full-term babies, having healthy mothers and normal Apgar scores, suspected of sepsis and candidates for antibiotic treatment in the NICU of Vali-e Asr Hospital. Exclusion criteria: Infants with positive blood cultures, infants with positive cerebrospinal fluid culture, infants being treated with corticosteroids, infants whose mothers were treated with corticosteroids or magnesium sulphate at least one week prior to delivery, infants whose mothers received antibiotics prior to delivery, cord acidosis and birth asphyxia, infants that are intravenously fed, and infants of ill mothers.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
IL-1ß. Timepoint: just before and 12 hrs after intervention. Method of measurement: ELISA,pg/ml.;IL-6. Timepoint: just before and 12 hrs after intervention. Method of measurement: ELISA,pg/ml.;IL-8. Timepoint: just before and 12 hrs after intervention. Method of measurement: ELISA,pg/ml.;TNF-a. Timepoint: just before and 12 hrs after intervention. Method of measurement: ELISA,pg/ml.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGolnaz Rezaeizadeh

Maternal Fetal Neonatal Research Center,Tehran University of Medical Sciences

golnaz_rezaei80@yahoo.com+98 21 6659 1316

Outcome results

None listed

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