Treatment and Vaccine Development of Mycoplasma Pneumoniae
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT03911440 |
Recruitment Status :
Recruiting
First Posted : April 11, 2019
Last Update Posted : April 11, 2019
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Condition or disease | Intervention/treatment | Phase |
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Atypical Pneumonia | Drug: Doxycycline Drug: Azithromycin | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 100 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Diagnosis and Treatment of Mycoplasma Pneumoniae and Vaccine Development |
Actual Study Start Date : | November 10, 2018 |
Estimated Primary Completion Date : | December 31, 2022 |
Estimated Study Completion Date : | December 31, 2022 |

Arm | Intervention/treatment |
---|---|
Active Comparator: Azithromycin
Azithromycin (10mg/kg/day) is given to children with mycoplasma pneumonia for 3 days.
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Drug: Azithromycin
Azithromycin is given with a dosage of 10 mg/kg/day once a day for 3 days. |
Experimental: Doxycycline
Doxycycline (2-4mg/kg/day) is given to children with mycoplasma pneumonia for 5-10 days.
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Drug: Doxycycline
Oral doxycycline is given with a dosage of 2-4 mg/kg/day divided into twice a day for 5-10 days. |
- Defervescence [ Time Frame: Up to 10 days ]The timing (days) when fever subsides after treatment
- Hospital stay [ Time Frame: Up to 2 weeks ]The length of hospitalization

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Ages Eligible for Study: | up to 18 Years (Child, Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- 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.
Exclusion Criteria:
- None

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03911440
Contact: Li-Min Huang, MD, PhD | 886-2-23123456 ext 71525 | lmhuang@ntu.edu.tw |
Taiwan | |
National Taiwan University Hospital | Recruiting |
Taipei, Taiwan, 100 |
Responsible Party: | National Taiwan University Hospital |
ClinicalTrials.gov Identifier: | NCT03911440 |
Other Study ID Numbers: |
201712045MINA |
First Posted: | April 11, 2019 Key Record Dates |
Last Update Posted: | April 11, 2019 |
Last Verified: | April 2019 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Mycoplasma pneumoniae, Macrolide-resistance, Children |
Mycoplasma Infections Pneumonia, Mycoplasma Pneumonia Pleuropneumonia Lung Diseases Respiratory Tract Diseases Respiratory Tract Infections Pleurisy Pleural Diseases Mycoplasmatales Infections |
Gram-Negative Bacterial Infections Bacterial Infections Pneumonia, Bacterial Azithromycin Doxycycline Anti-Bacterial Agents Anti-Infective Agents Antimalarials Antiprotozoal Agents Antiparasitic Agents |