Can a spoonful of yoghurt calm the Body's fire in the ICU?
NCT ID NCT07812415
First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time
Summary
This pilot trial asks whether adding plain yoghurt to standard tube feeding is safe and practical for adults who are critically ill in the intensive care unit. Twelve patients receive either yoghurt or usual care for three days. Researchers track inflammation markers and changes in gut bacteria to see if yoghurt shows early signs of helping.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- plain yoghurt given through a feeding tube
- What this could lead to
- If yoghurt helps, it could offer a simple, low-cost way to calm inflammation and support gut bacteria in people who are critically ill and fed through a tube.
- What could go wrong
- This is a tiny pilot study of 12 people, so any inflammation or microbiome changes may be chance or may not hold in a larger group. Yoghurt can cause digestive upset or allergic reactions in people sensitive to dairy.
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
-
12 people
The number who actually took part.
- Started
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Jun 2021
- Finished
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Aug 2021
- Lead sponsor
-
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
-
18 to 65 years
- Sex
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Anyone
- Healthy volunteers
-
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: * Adults aged 18-65 years Admitted to Intensive Care Unit (ICU) with critical illness requiring nasogastric feeding Expected to remain in ICU for at least 3 days Able to receive enteral nutrition via nasogastric tube Exclusion Criteria: * Known allergy or intolerance to dairy products Pre-existing gastrointestinal disorders (e.g., inflammatory bowel disease, short bowel syndrome) Severe liver disease or renal failure requiring dialysis Immunocompromised state (e.g., HIV/AIDS, chemotherapy) Participation in another interventional clinical trial within the past 30 days
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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
-
All India Institute of Medical Sciences (AIIMS) Bhubaneswar
Bhubaneswar, Odisha, 751019, India
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