A shot against the shakes: could a Low-Dose drug stop Post-Surgery shivering?
NCT ID NCT07787702
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This trial tests whether a small dose of ketamine or tramadol, given right after spinal anesthesia, can prevent the shivering that often follows. It includes adults aged 18 to 60 undergoing orthopedic surgery. The study compares how often and how severely shivering occurs with each drug, aiming to find a better way to keep patients comfortable.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Low-dose intravenous ketamine or tramadol given right after spinal anesthesia to prevent shivering.
- What this could lead to
- If effective, this could identify a better preventive option for post-anesthesia shivering, improving patient comfort during recovery.
- What could go wrong
- This is a small, early-stage trial, and results may not apply broadly. Both drugs carry potential side effects, and the optimal dose or benefit may not be confirmed.
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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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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About 106 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Feb 2027
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.
- Ages
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18 to 60 years
- 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: * \* ASA I and II patients aged 18-60 years. * Both genders. * Patients undergoing orthopedic surgery under spinal anesthesia. Exclusion Criteria: * \* Patient refusal. * ASA III and ASA IV. * Prolonged surgical procedures expected to be more than 90 minutes. * Patients who received blood transfusion or study drugs other than for the study purpose.
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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 places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Shaheed Mohtarma Benazir Bhutto Institute of Trauma (SMBBIT)
Karachi, Sindh, 74200, Pakistan