AI could forecast spinal block duration, study tests
NCT ID NCT07816003
First seen Sep 11, 2026 · Last updated Sep 16, 2026 · Updated 3 times
Summary
Spinal anesthesia wears off at different speeds in different people, even when they get the same dose. Researchers are building machine learning models to predict how long sensory and motor blocks will last in adults having elective surgery. The study will record body measurements and clinical details before surgery, then track block regression afterward. The goal is a practical tool to help anesthesiologists plan cases and discharges.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If the models work, anesthesiologists could estimate how long a spinal block will last for each patient, which may help with scheduling surgeries and planning discharge.
- What could go wrong
- This is an observational study that only builds and tests prediction models on a single group of patients. The models may not work well in other hospitals or patient groups, and they cannot replace clinical judgment.
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.
- Participants
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About 255 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2028
An estimate. End dates often move.
- 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.
Who is studied
Consecutive adults scheduled for elective surgery under single-shot spinal anaesthesia at Specialized Medical Center, King Fahad campus, Riyadh.
- Ages
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18 years and older
- Sex
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Anyone
- 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: * Adults scheduled for elective surgery under single-shot spinal anaesthesia * ASA physical status I to III * Written informed consent obtained Exclusion Criteria: * Contraindication to neuraxial anaesthesia (coagulopathy, local or systemic infection, raised intracranial pressure, patient refusal) * Failed or incomplete block requiring conversion to general anaesthesia * Repeated or top-up intrathecal injection * Pregnancy * Known spinal deformity or previous spine surgery * Pre-existing neurological or neuromuscular disease affecting sensory or motor assessment * Inability to cooperate with sensory and motor assessment
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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