Small study seeks best dose of anesthesia booster for joint surgery
NCT ID NCT07144215
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This completed study with 40 adults undergoing hip or knee surgery aimed to find the most effective dose of dexmedetomidine when added to standard spinal anesthesia. Researchers tested doses from 3 to 6 micrograms to see which one made the numbness last at least 200 minutes. The goal is to improve pain control during and after surgery.
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 successful, this could help doctors choose the right dose of dexmedetomidine to make spinal anesthesia last longer during hip and knee surgery.
- What could go wrong
- This is a small, early-phase study with only 40 participants, so results may not apply to everyone. The main risks include low blood pressure, slow heart rate, and nausea.
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
-
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
-
40 people
The number who actually took part.
- Started
-
Feb 2025
- Finished
-
May 2025
- 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
-
18 to 60 years
- Sex
-
Anyone
- Healthy volunteers
-
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: * 18-60 years old * Pelvic or knee surgery patient with American Society of Anesthesiologists physical status I - III with epidural spinal anesthesia * Body mass index 18-35 kg/m2 * Body height 150-180 cm * Willing to become a research participant Exclusion Criteria: * Have a history of allergy to bupivacaine or dexmedetomidine * Have sensory or motoric disabilities in the lower extremity contralateral to the surgery area * Have a history of congestive heart failure and/or heart rhythm disorder * Have regional anesthesia contraindication
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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
-
RSUPN Cipto Mangunkusumo
Jakarta Pusat, Jakarta Special Capital Region, 10430, Indonesia
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a simple drug stop nausea during emergency C-Sections?
- Side-Lying after spinal anesthesia may protect elderly patients from dangerous blood pressure drops
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- New knee pain block could get you walking faster after surgery
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