Skip to content

NSAIDs Treatment in Children With Pleuropneumonia

The Role of Non Steroidal Anti Inflammatory Drugs in the Treatment of Pleuropneumonia in Children. a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01586299
Enrollment
40
Registered
2012-04-26
Start date
2012-03-31
Completion date
2015-06-30
Last updated
2014-11-14

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

Conditions

Pleuro-pneumonia

Keywords

pleuropneumonia children, non steroidal anti inflammatory drugs, pleural effusion, severe pneumonia

Brief summary

The purpose of this study is to evaluate the influence of routine NSAIDs treatment for hospitalized children with pleuropneumonia in comparison with acetominophen treatment (all in conjunction with adequate antibiotic therapy).

Interventions

DRUGIbuprofen

10 mg/kg every 8 hours until 24 hours after resolution of fever

DRUGAcetaminophen

15 mg/kg every 6 hours until 24 hours after resolution of fever

Sponsors

Rabin Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
No

Inclusion criteria

* age less than 18 years * admission in Schneider childrenMC of Israel, wards a/c * clinical diagnosis of pneumonia with evidence of pleural effusion on chest X-ray * parental informed consent * follow-up ability after discharge

Exclusion criteria

* pneumonia secondary to foreign body aspiration * immune deficiency * chronic lung disease other than asthma (CF, CLD of prematurity, Familial Dysautonomia, etc) * significant premorbidity (organ failure, rheumatic disease, etc) * endotracheal/endobronchial devices including tracheostomy. * parental refusal to participate in the study.

Design outcomes

Primary

MeasureTime frame
clinical improvement as manifested by resolution of fever and length of hospital admission.participants will be followed for the duration of hospital stay, an expected average of 10 days

Secondary

MeasureTime frame
clinical improvement as manifested by respiratory parameters (tachypnea, dyspnea, Fio2),and inflammatory markers.participants will be followed for the duration of hospital stay, an expected average of 10 days

Countries

Israel

Contacts

Primary Contactshai ashkenazi, Prof
sashkenazi@clalit.org.il972-3-9253680
Backup Contacthavatzelet yarden-bilavsky, Dr
yojiby@gmail.com972-54-6777054

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026