Clinical Trials Directory

Trials / Terminated

TerminatedNCT01217099

Methylprednisolone Pulse Macrolide Therapy for Refractory Mycoplasma Pneumoniae Pneumonia in Children

A Prospective, Open-label Trial of Methylprednisolone Pulse Macrolide Therapy for Refractory Mycoplasma Pneumoniae Pneumonia in Children

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
47 (actual)
Sponsor
Chongqing Medical University · Academic / Other
Sex
All
Age
3 Years – 11 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is planned to investigate whether small doses of methylprednisolone pulse macrolide therapy can relieve symptoms,chest X-rays faster than macrolide alone therapy for refractory mycoplasma pneumoniae pneumonia(MPP) .

Detailed description

Corticosteroid has been used in adulthood refractory MPP with satisfactory efficacy. But there were few studies about the use of corticosteroid in children with refractory MPP. Lee KY et al indicated oral prednisolone of 1 mg/kg/ day for 1 week be useful for children with severe MPP. Akihiro T et al demonstrated that intravenously administered methylprednisolone at a dose of 30 mg/kg once daily for 3 consecutive days had an efficacious treatment for children with refractory MPP.But the methods of corticosteroid use, such as the dosage, administration route, duration of treatment have not been well understood. So in this study, we planned to investigate whether small doses of methylprednisolone pulse macrolide therapy can relieve symptoms,chest X-rays faster than macrolide alone therapy for refractory mycoplasma pneumoniae pneumonia in a prospective, open-label fashion. PMID: 11096025 PMID: 18033831 PMID: 10434547 PMID: 16437541 PMID: 18656264

Conditions

Interventions

TypeNameDescription
DRUGmethylprednisolonetreatment patients were iv methylprednisolone pulse azithromycin for 5 days.
DRUGazithromycincontrol patients were iv azithromycin for 5 days.

Timeline

Start date
2007-05-01
Primary completion
2010-05-01
Completion
2010-05-01
First posted
2010-10-08
Last updated
2010-10-08

Source: ClinicalTrials.gov record NCT01217099. Inclusion in this directory is not an endorsement.