Study aims to perfect epidural dose for faster labor pain relief
NCT ID NCT07076368
First seen Jan 28, 2026 · Last updated Jun 22, 2026 · Updated 17 times
Summary
This study tests different amounts of a common epidural medicine (ropivacaine and fentanyl) to find the dose that works best within 30 minutes for women in labor. About 50 pregnant women with a single baby in active labor will receive the epidural through a special technique. Researchers will measure pain scores and side effects to improve pain relief during childbirth.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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University of California, San Francisco
RECRUITINGSan Francisco, California, 94158, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
Ropivacaine and fentanyl (epidural)
What this could lead to
If successful, this could help doctors use the smallest effective dose of epidural medicine for faster, safer labor pain relief.
What could go wrong
This is a small, early-phase study focused on dosing, not a new treatment. Results may not apply to all women, and side effects like low blood pressure or itching are possible.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.