Brain surgery pain showdown: which drug wins?
NCT ID NCT07254936
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study tested two pain medicines, ketamine and dexmedetomidine, in 38 adults recovering from brain surgery in the ICU. Researchers measured pain levels using a special tool at 6, 12, and 24 hours after treatment. The goal was to see which drug provides better pain relief for these patients.
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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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38 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Apr 2025
- 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 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.
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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: * Patients aged 18 years and older. * Intubated post-craniotomy patients in the ICU. * Glasgow Coma Scale (GCS) score of 8-15 pre-operatively. Able to provide informed consent (either personally or through family/legal representative). Exclusion Criteria: * Hypersensitivity to ketamine or dexmedetomidine. * Renal failure (elevated serum creatinine and BUN). * Heart failure (EF \<40%, elevated BNP/NT-proBNP, abnormal ECG). * Hepatic failure (elevated AST/ALT, bilirubin, prolonged PT/INR). * Patients with severe bradycardia, hypotension, or hallucinations due to study drugs. * Death during the study period. * New critical illness (e.g., sepsis, stroke). * Withdrawal of consent by the patient or family. * Incomplete data or ICU discharge before 24-hour follow-up.
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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.
Contacts and locations
Locations
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H. Adam Malik General Hospital, Hajj General Hospital, and TK II Putri Hijau Army Hospital
Medan, North Sumatra, 20155, Indonesia
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