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Completed

NCT Number: NCT02149433

Pneumocystis Jerovici Pneumonia in Infants and Steroids

This is a double-blind randomized controlled trial assessing the efficacy of adjuvant corticosteroids in clinically diagnosed Pneumocystis jiroveci pneumonia in infants.

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Key information

Age range

2 month–6 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Queen Elizabeth Central Hospital

Blantyre, Malawi

About this study

The study aims to determine whether the early administration of adjuvant corticosteroids in addition to high dose oral Co-trimoxazole reduces mortality amongst infants aged 2-6 months with vertically acquired HIV and clinically diagnosed Pneumocystis jiroveci pneumonia. Infants will be randomized to receive either a steroid regime of oral prednisolone at 2 mg/kg for 7 days, then 1 mg/kg for 7 days, then 0.5mg/kg for 7 days for a total of 21 days or placebo.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Consecutive infants with HIV and clinical features of Pneumocystis jiroveci pneumonia who require oxygen (oxygen saturations in air < 90%).
  • Clinical diagnosis of Pneumocystis jiroveci pneumonia will be made by one of the study investigators. All infants must be HIV ELISA positive or exposed, have an oxygen requirement (saturations on air < 90%) and have severe respiratory distress and cough. They may also have a low grade fever, clear chest or diffuse signs on auscultation and features suggestive of Pneumocystis jiroveci infection on chest radiography.

Exclusion criteria

  • Previous known allergy or hypersensitivity or other contraindication to corticosteroids or co-trimoxazole.
  • Previous treatment for suspected Pneumocystis jiroveci pneumonia or a delay starting steroids for greater than 24 hours after starting high dose co-trimoxazole.
  • Patients who are not exposed to HIV.
  • Infants with known preexisting active pulmonary or cardiac disease.
  • Patients who do not live within the Blantyre district and who are unable to attend follow up at QECH.
  • Infants whose parents or guardians refuse consent.

Treatment and study plan

Prednisone

Drug

The steroid regime will be oral prednisone at 2 mg/kg for 7 days, then 1 mg/kg for 7 days, then 0.5mg/kg for 7 days for a total of 21 days.

Placebo

Drug

Primary outcomes

  1. Reduction in inpatient mortality by 20%.

    Time frame: 36 months

    To determine whether the addition of oral Prednisolone to standard treatment reduces inpatient mortality by 20% in patients aged 2-6 months with clinical PJP pneumonia.

Secondary outcomes

  1. Commencement of antiretroviral treatment

    Time frame: 36 months

    To determine whether steroids significantly increase the number of patients that successfully commence anti-retroviral treatment.

  2. 6 month survival

    Time frame: 36 months

    To determine whether steroids significantly increase the number of patients that survive to 6 months following commencement of anti-retrovirals.

  3. Morbidity (days in hospital and days on oxygen)

    Time frame: 36 months

    To determine whether steroids significantly alter morbidity as determined by number of days spent in hospital as an inpatient and number of days on oxygen.

Sponsors and collaborators

Lead sponsor

Kamuzu University of Health Sciences

Other

Registry information

Official study title

Early Steroid Use in Infants With Clinical Pneumocystis Jiroveci Pneumonia (PCP) in the Queen Elizabeth Central Hospital, Blantyre, Malawi

Important dates

Study start
2012
Primary completion
2014
Study completion
2015
First posted
May 29, 2014
Registry last updated
Dec 11, 2015

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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