Treatment and Vaccine Development of Mycoplasma Pneumoniae
Diagnosis and Treatment of Mycoplasma Pneumoniae and Vaccine Development
1 other identifier
interventional
100
1 country
1
Brief Summary
A randomized clinical trial comparing treatment effectiveness of azithromycin and doxycycline for pediatric Mycoplasma pneumonia.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2018
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 10, 2018
CompletedFirst Submitted
Initial submission to the registry
April 9, 2019
CompletedFirst Posted
Study publicly available on registry
April 11, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2022
CompletedApril 11, 2019
April 1, 2019
4.1 years
April 9, 2019
April 9, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Defervescence
The timing (days) when fever subsides after treatment
Up to 10 days
Secondary Outcomes (1)
Hospital stay
Up to 2 weeks
Study Arms (2)
Azithromycin
ACTIVE COMPARATORAzithromycin (10mg/kg/day) is given to children with mycoplasma pneumonia for 3 days.
Doxycycline
EXPERIMENTALDoxycycline (2-4mg/kg/day) is given to children with mycoplasma pneumonia for 5-10 days.
Interventions
Oral doxycycline is given with a dosage of 2-4 mg/kg/day divided into twice a day for 5-10 days.
Azithromycin is given with a dosage of 10 mg/kg/day once a day for 3 days.
Eligibility Criteria
You may qualify if:
- Children aged 0-18 years, admitted due to lower respiratory tract infections. Mycoplamsa pneumonia is diagnosed.
- The diagnosis is made within 72 hours after fever onset.
- The patient and his/her guardians are willing to participate the study and able to follow the instruction.
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Taiwan University Hospital
Taipei, 100, Taiwan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 9, 2019
First Posted
April 11, 2019
Study Start
November 10, 2018
Primary Completion
December 31, 2022
Study Completion
December 31, 2022
Last Updated
April 11, 2019
Record last verified: 2019-04
Data Sharing
- IPD Sharing
- Will not share