Could a simple Add-On drug make C-Section recovery smoother?
NCT ID NCT05991466
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether adding dexmedetomidine to standard spinal anesthesia or a TAP block (a type of pain injection) improves recovery quality and pain relief for women having planned C-sections. 141 full-term pregnant women participated. The goal was to see if the drug leads to better recovery scores and longer time before needing additional pain medication.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Dexmedetomidine (added to bupivacaine in spinal anesthesia or TAP block)
- What this could lead to
- If it works, this could lead to better recovery and longer pain relief after planned C-sections.
- What could go wrong
- This is a small, completed Phase 4 trial, so results may not apply to all women. The drug may cause side effects like sedation or low blood pressure.
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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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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141 people
The number who actually took part.
- Started
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Jan 2022
- Finished
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Dec 2022
- 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
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18 to 40 years
- 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.
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: * Participants will be full-term pregnant females * ASA classification I or ll. * Aged between 18 and 40 years. * Singleton pregnancy Exclusion Criteria: * Refusal of block. * Bleeding disorders (platelets count \<150,000; INR\>1.5; PC\<60%). * wounds or infection at the puncture site. * Known allergy to local anesthetic drugs. * Contraindications to neuroaxial block. * Contraindications to TAP block..
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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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Faculty of Medicine, Cairo University
Cairo, Cairo Governorate, 11562, Egypt