Color doppler could make epidurals safer for moms in labor
NCT ID NCT05606952
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether color Doppler ultrasound can accurately show where the epidural pain-relief medicine flows in laboring women. Researchers studied 194 women to see how well this technique detects correct catheter placement. The goal is to improve safety and effectiveness of epidurals during childbirth.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could provide a reliable, non-invasive way to confirm correct epidural placement, reducing failed blocks and complications.
- What could go wrong
- This is a small, completed observational study. Results may not apply to all hospitals or patients, and the technique requires training and equipment.
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.
- Participants
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194 people
The number who actually took part.
- Started
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Dec 2022
- Finished
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Nov 2023
- 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.
Who is studied
labouring pregnant women aged 18-45 years with a singleton gestation requesting epidural analgesia.
- Ages
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18 to 45 years
- Sex
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Female participants only
- 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: * obstetric patients admitted for epidural analgesia in the labor department suite (LDS) Exclusion Criteria: 1. Patients suffering from coagulopathy. 2. Patients on recent anticoagulant therapy. 3. Patients suffering from sepsis or with local sepsis at the insertion site. 4. Patients with platelet count less than 100,000/dl. 5. Patient refusal. 6. Patient with known allergy to local anesthetic drugs 7. Patients delivered by forceps. 8. Patients who have undergone a cesarean section delivery.
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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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Menoufia University
Menoufia, Menoufia, 32817, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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