Could a tiny dose of dexmedetomidine double Pain-Free time after surgery?
NCT ID NCT07651488
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This trial tests whether adding a small dose of dexmedetomidine to a standard spinal anesthetic (bupivacaine) can extend pain relief for adults undergoing perianal surgery. One hundred participants aged 40–80 will receive either the standard anesthetic alone or with dexmedetomidine. The main goal is to see how long pain relief lasts and whether it reduces the need for 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
- What this could lead to
- If it works, this could provide longer-lasting pain relief after perianal surgery, reducing the need for additional painkillers.
- What could go wrong
- This is a very early-phase trial with only 100 participants, so results may not apply broadly. Adding dexmedetomidine may also increase side effects like drowsiness 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
-
Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
-
100 people
The number who actually took part.
- Started
-
Mar 2023
- Finished
-
Sep 2023
- 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
-
40 to 80 years
- Sex
-
Anyone
- Healthy volunteers
-
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: * Patients undergoing elective perianal surgery under spinal saddle block were included in the study. * Age between 40-80 years * ASA status I and II Exclusion Criteria: * Pregnant women * Patient with coagulopathy * Infection at or near the needle insertion site * Allergy to the trial drug * Patient with chronic pain * Cognitive impairment * Patient with known drug or substance abuse
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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
-
Liaquat National Hospital
Karachi, Pakistan
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