Which drug restores blood pressure faster in children with septic shock?
NCT ID NCT07775001
First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time
Summary
This trial compares two emergency medications, dopamine and epinephrine, to see which one is better at reversing septic shock in children aged 2 to 12. Septic shock is a life-threatening condition where infection causes dangerously low blood pressure. The study randomly assigns children who haven't improved with fluids to receive either drug, then checks if blood pressure and other signs of shock improve within the first hour. The goal is to find out if one drug works faster and more effectively, which could guide emergency treatment for children worldwide.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- epinephrine and dopamine
- What this could lead to
- If epinephrine works better, it could become the preferred first-line treatment for children with septic shock, potentially saving more lives.
- What could go wrong
- This is a small, early-stage trial, so results may not apply to all children. Both drugs have risks like abnormal heart rhythms, and the study doesn't guarantee long-term benefits.
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
-
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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66 people
The number who actually took part.
- Started
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Feb 2026
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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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2 to 12 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Children aged 2 to 12 years, of either sex, presenting to the Pediatric Emergency Department or Pediatric Intensive Care Unit. * Suspected or proven infection, supported by a documented clinical focus of infection or microbiological evidence. * Fluid-refractory hypotensive septic shock . Exclusion Criteria: * Shock not meeting the operational definition of fluid-refractory hypotensive septic shock after standardized fluid resuscitation. * Receipt of any vasoactive infusion, including dopamine, epinephrine, norepinephrine, vasopressin, dobutamine, or equivalent, before eligibility confirmation and randomization. * Known cyanotic congenital heart disease, significant structural heart disease with hemodynamic compromise, or documented cardiomyopathy. * Primary arrhythmic instability requiring antiarrhythmic therapy at presentation. * Anaphylaxis, acute hemorrhage, major trauma, or obstructive shock, such as tension pneumothorax or cardiac tamponade, as the primary cause of hypotension. * Clinical indication for an alternative initial vasoactive strategy mandated by the treating team at screening, including predominant warm vasodilatory shock requiring norepinephrine as first-line therapy. * Documented limitation of care orders, including do-not-resuscitate status, or anticipated withdrawal of life-sustaining therapy at presentation.
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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.
Contacts and locations
Locations
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Nishtar Hospital Multan
Multan, Punjab Province, 66000, Pakistan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- A new blood marker may outperform lactate in predicting septic shock survival