Spinal anesthesia showdown: which additive offers better comfort for kidney stone surgery?
NCT ID NCT06957301
First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time
Summary
This trial tests whether adding fentanyl or dexmedetomidine to standard spinal anesthesia improves patient satisfaction and sedation during kidney stone surgery. Sixty adults aged 18–60 undergoing the procedure will receive one of the two combinations. The goal is to find which additive provides better pain control and a smoother recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- fentanyl and dexmedetomidine
- What this could lead to
- If one combination works better, it could offer a more comfortable and safer anesthesia option for kidney stone surgery.
- What could go wrong
- This is a small, early-stage trial with only 60 participants, so results may not apply to everyone. Both drugs have known side effects like nausea 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
-
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
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60 people
The number who actually took part.
- Started
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Apr 2025
- Finished
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Mar 2026
- 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.
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * both sex aged between 18 and 60 years, * belonging to American Society of Anaesthesiologists (ASA) physical status Grade I and II undergoing PCNL under spinal anaesthesia. Exclusion Criteria: * Patients with a history of spine surgery, * infection at the injection site, * coagulopathy, * hypovolemia, * increased intracranial pressure, * indeterminate neurologic disease, * spinal deformities, * communication problems, * known hypersensitivity to local anaesthetics, opioids or dexmedetomidine
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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
-
Faculty of medicine ,Alexandria university
Alexandria, Alexandria Governorate, 21521, Egypt
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