Could a shorter steroid course be just as good for HIV-Related pneumonia?
NCT ID NCT03856229
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares a shortened steroid regimen (8 days for moderate, 14 days for severe pneumonia) against the standard 21-day course in 196 HIV patients with Pneumocystis pneumonia. The goal is to see if the shorter treatment is non-inferior in preventing death and complications. Participants must be on standard antibiotics and start steroids within 48 hours of admission.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- prednisolone (or methylprednisolone equivalent)
- What this could lead to
- If successful, this could show that a shorter steroid course is just as effective, reducing side effects and simplifying treatment for HIV patients with this type of pneumonia.
- What could go wrong
- This is a non-inferiority trial, so it may only confirm that the shorter course is not worse, not necessarily better. The results may not apply to patients with other health conditions or those not on standard antibiotics.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 196 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2019
- Expected to finish
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Jul 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Older than 18 years * To have a gasometry at the admission that confirms moderate or severe PCP. * Patients receiving trimethoprim / sulfamethoxazole in doses of 15 to 20 mg / kg per day from the first 24 hours after admission. * Patients who have begun adjuvant treatment with steroids in the first 48 hours after admission. * No history of chronic pulmonary disease. * APACHE at hospitalization less than 20 points. Exclusion Criteria: * Allergic to TMP/SMX, who have not tolerated desensitization. * History of inflammatory, infectious, autoimmune or neoplastic diseases except Kaposi's sarcoma, which merit the chronic use of steroids. * Pleural or pericardial effusion and meningitis from any cause. * Septic shock not related to PCP. * Subjects who during the hospitalization have been diagnosed with any neoplasia (except Kaposi´s sarcoma)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Centro de Investigacion en Enfermedades Infecciosas
México, State of Mexico, 14080, Mexico
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