Could a single dose of ketamine during heart surgery stop Long-Term pain?
NCT ID NCT07490457
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will test whether giving a single dose of ketamine during open-heart surgery can reduce chronic pain that often lingers for months after the operation. Researchers will compare 100 adults who receive either ketamine or a placebo during surgery, then track their pain levels and painkiller use for up to 6 months. If successful, this simple addition to anesthesia could improve recovery and reduce reliance on opioids.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ketamine
- What this could lead to
- If it works, this could point toward a simple way to prevent long-term pain after open-heart surgery and reduce the need for strong painkillers.
- What could go wrong
- This is a small, early-stage trial (100 people) that hasn't started yet. The results may not apply to all heart surgery patients, and ketamine can cause side effects like confusion or hallucinations.
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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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May 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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 80 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 II-III, * Patients scheduled for elective on-pump open cardiac surgery via median sternotomy. Exclusion Criteria: * Emergency surgery requirement * Need for reoperation * Requirement for postoperative re-intubation * History of opioid use * Preoperative diabetic neuropathy or autonomic dysfunction * Hepatic or renal dysfunction * History of neuropathic pain * Neurocognitive disorders such as psychosis or dementia * Use of antidepressants or antipsychotics * Body mass index (BMI) \> 40
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Conditions
The condition(s) this trial relates to.
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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Bursa City Hospital,
Bursa, nilüfer, Turkey (Türkiye)
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