Warming blankets and fluids tested to prevent hypothermia in C-Section births
NCT ID NCT05015582
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested different warming methods—like forced air blankets and warmed IV fluids—to prevent hypothermia in women having planned C-sections. Only 16 women participated before the trial was stopped early. The goal was to see which method best keeps mother and baby warm and reduces complications like shivering.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- forced air warming blankets and warmed IV fluids
- What this could lead to
- If successful, this could point to a simple, low-cost way to keep mothers and newborns safer during C-sections by preventing hypothermia.
- What could go wrong
- The trial was terminated early with very few participants, so results are not reliable. Warming methods may not make a meaningful difference in outcomes.
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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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16 people
The number who actually took part.
- Started
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Aug 2021
- Finished
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Dec 2021
- 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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Female participants only
- 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: * scheduled for elective cesarean section under neuraxial anesthesia * singleton pregnancy Exclusion Criteria: * gestational age of less than 37 week * emergency cesarean
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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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The University of Texas Health Science Center at Houston
Houston, Texas, 77030, United States
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