Simulation drills aim to sharpen Doctors' skills in postpartum emergencies
NCT ID NCT07519252
First seen Jun 27, 2026 · Last updated Jul 29, 2026 · Updated 4 times
Summary
This study will test whether a simulation-based training program helps senior anesthesiology residents better manage postpartum hemorrhage, a life-threatening bleeding emergency after childbirth. Thirty-six residents will undergo high-fidelity simulation training, and their teamwork, communication, and decision-making skills will be measured before and after. The goal is to see if this type of training improves crisis management in obstetric emergencies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Simulation-based postpartum hemorrhage training
- What this could lead to
- If successful, this could show that simulation training helps doctors respond better to dangerous bleeding after childbirth, potentially improving patient safety.
- What could go wrong
- This is a small, early study with only 36 participants, and it measures skills in a simulated setting, not real patient outcomes. Results may not translate to actual emergencies.
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 36 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 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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24 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Senior anesthesiology residents * Currently working in the department of anesthesiology and reanimation * Voluntary participation in the study Exclusion Criteria: * Refusal to participate * Incomplete participation in the simulation session
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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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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Hacettepe University Faculty of Medicine
RECRUITINGAnkara, Ankara, 06100, Turkey (Türkiye)
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- Medical glue vs. internal bleeding: a new hope?
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