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NCT Number: NCT02303587

Methylprednisolone for Children With Severe Mycoplasma Pneumoniae Pneumonia (MCMP)

The study is designed to investigate difference in percentage of presentation of atelectasis, bronchiectasis, bronchiolitis obliterans, or consolidation in 6 months after discharge in those treated with a low dose regimen of methylprednisolone initiated with 2 or 4 mg/kg/d for 3 days followed by tapering, combined with sequential treatment with azithromycin versus a high dose regimen of methylprednisolone initiated with 10 mg/kg/d for 3 days followed by tapering, combined with sequential treatment with azithromycin.

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Key information

Age range

29 day–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Beijing Children's Hospital, Capital Medical University

Beijing, Beijing Municipality, 100045, China

About this study

Mycoplasma pneumonia pneumonia (MPP) accounts for approximately 10-30% of childhood community-acquired pneumonia (CAP) in China. Macrolide is the first choice for MPP. However, progression to severe pneumonia might occur despite antibiotics therapy. And some patients have sequelae of bronchiolitis obliterans, bronchiectasis and atelectasis, et al. Based on inflammatory and immunological mechanism, there is some clinical evidence that adjuvant of corticosteroid reduced morbidity and improved the outcome in the children with severe MPP. However, the dosage of corticosteroid varied greatly in studies. Therefore, a large prospective study is needed to define the benefits of high-dose corticosteroid therapy in MPP.

Patients will be randomized into two groups: the low dose group and the high dose group. The low dose group will receive methylprednisolone 2 or 4 mg/kg/d for 3 days followed by tapering in 9 days, combined with sequential treatment with azithromycin. The high dose group will receive methylprednisolone 10 mg/kg/d for 3 days followed by tapering in 9 days, combined with sequential treatment with azithromycin. After discharge, patients of both groups will be followed up at 1, 3, and 6 months.

The number of pulmonary lesions, including atelectasis, bronchiectasis, bronchiolitis obliterans, or consolidations, in 6 months after discharge will be compared in two groups. The number of adverse events, such as hyperglycemia, hypertension, increased intraocular pressure, will be compared between the two groups.

The trial will be completed in 36 months, with 424 subjects recruited from 5 hospitals in partnership with clinical research collaboration of National Clinical Research Center for Respiratory Diseases.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Severe pneumonia diagnosis criteria were based on the "Zhu Futang Practical Pediatrics" (the 7th Edition) and "the guideline of management of community-acquired pneumonia in children in China"(Chinese Journal of Pediatrics, 2013, 51:745-752, 856-862). Severe pneumonia is defined as pneumonia with one of the following:

  • Less than 18 years old
  • Severe pneumonia that is defined as pneumonia with one of the followings:
  • poor general condition
  • increased respiratory rate( infant>70/min,older children>50/min)
  • dyspnea
  • cyanosis
  • multilobe involvement or ≥ 2/3 lung involvement
  • extrapulmonary complication
  • pleural effusion
  • Transcutaneous oxygen saturation in room air ≤92%
  • Serum M. pneumoniae antibody≥ 1:320, or serum M. pneumoniae antibody≥ 1:160 with positive PCR of M. pneumoniae or seroconversion (increased antibody titers ≥4 folds) Subject/Guardian is informed and consent.

Exclusion criteria

Subject will be excluded if she or he has one of the following:

  • evidence of bacterial pneumonia;
  • evidence of viral pneumonia;
  • evidence of fugal pneumonia;
  • evidence of pulmonary tuberculosis;
  • respiratory failure requiring mechanical ventilation;
  • hemophagocytic syndrome;
  • liver failure or renal insufficiency;
  • congenital heart disease;
  • heart failure;
  • kidney disease;
  • connective tissue disease;
  • immunodeficiency;
  • tumor;
  • a history of hypertension or diabetes mellitus;
  • recurrent respiratory tract infection;
  • congenital bronchopulmonary dysplasia;
  • increased intraocular pressure;
  • history of use of glucocorticoids ≥1 week in previous 3 months;
  • having contraindications to glucocorticoids or azithromycin;
  • using of immunosuppressant before randomization;
  • undergoing trial for other medications or instruments.

Treatment and study plan

methylprednisolone

Drug

Primary outcomes

  1. pulmonary lesions

    Time frame: 6 months

    Pulmonary lesions include atelectasis, bronchiectasia, bronchiolitis obliterans, consolidation

Secondary outcomes

  1. recovery time of temperature

    Time frame: 2 weeks

  2. the proportion of absorption of pulmonary lesions

    Time frame: 2 weeks

  3. duration of hospitalization,

    Time frame: 2 weeks

  4. number of participant(s ) need intensive care

    Time frame: 2 weeks

  5. number of participant(s )with acute respiratory distress syndrome

    Time frame: 2 weeks

  6. number of participant(s) with hemophagocytic syndrome

    Time frame: 2 weeks

  7. number of participant(s) with hyperglycemia

    Time frame: 2 weeks

  8. number of participant(s) with hypertension

    Time frame: 6 months

  9. number of participant(s) who died during the trial

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Beijing Children's Hospital

Other

Collaborators

  • Baoding Children's Hospital
  • Children's Hospital of The Capital Institute of Pediatrics
  • Shanxi Provincial Maternity and Children's Hospital
  • Shengjing Hospital

Registry information

Official study title

Low Dose Versus High Dose Methylprednisolone for Children With Severe Mycoplasma Pneumoniae Pneumonia : a Multicenter Randomized Blinded Trial

Important dates

Study start
2014
Primary completion
2019
Study completion
2019
First posted
Dec 1, 2014
Registry last updated
Jan 8, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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