Could a 1,000-Year-Old pill be the next breakthrough in stroke care?
NCT ID NCT07784569
First seen Aug 25, 2026 · Last updated Aug 26, 2026 · Updated 1 time
Summary
This trial tests whether adding a traditional Chinese medicine, Angong Niuhuang Pill, to standard stroke care can improve outcomes for adults who have just had a stroke. The study uses an adaptive platform design, allowing multiple treatments to be tested simultaneously and efficiently. The main goal is to see if the treatment reduces disability and improves recovery, measured by the modified Rankin Scale.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Angong Niuhuang Pill (ANP), a traditional Chinese medicine, given as an add-on to standard stroke care.
- What this could lead to
- If successful, this could identify a widely applicable treatment that improves recovery and reduces disability after stroke, potentially benefiting millions worldwide.
- What could go wrong
- The trial is large and adaptive, but results depend on many factors. The treatment may not show benefit over standard care, and there are risks associated with any new intervention in acute stroke.
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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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 20,000 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Feb 2030
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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18 years and older
- 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.
Platform Inclusion Criteria: * Age ≥18 years * Clinical diagnosis of stroke Platform Exclusion Criteria \- There are no platform level exclusion criteria Each state and domain will specify additional inclusion and exclusion criteria in the respective Domain-Specific Registration. Patients who fulfill the overall platform criteria will be assessed for enrollment into each active domain.
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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 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.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Correlation of visual and motor deficits in stroke patients
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- Brazilian version of a behavior change intervention to support healthy lifestyle adoption after stroke - iVIDAVC: protocol for a pilot randomized study
- Determination of efficacy of sustained motor contraction generated using StimWave peripheral nerve stimulator
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