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Colonoscopy sedation study: which drug is safer for Seniors' brains?
NCT ID NCT07384169
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study looked at 164 adults aged 65 and older who had a colonoscopy with sedation. Researchers compared two common sedatives—propofol and dexmedetomidine—to see how they affected thinking and memory. They also checked whether frailty played a role. Participants took a simple thinking test before the procedure and again 2 and 24 hours after. The goal was to find out which sedation method might be safer for older patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- propofol and dexmedetomidine
- What this could lead to
- If it works, this could help doctors choose the safest sedation method for older adults undergoing colonoscopy to protect their thinking skills.
- What could go wrong
- This is a small, completed observational study, not a large trial. Results may not apply to all older adults or other procedures.
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
-
164 people
The number who actually took part.
- Started
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Aug 2023
- Finished
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Jan 2024
- 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
65 years and older
- Ages
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65 years and older
- 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.
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: * Age ≥65 years * Elective colonoscopy * ASA physical status I-III * Provision of written informed consent Exclusion Criteria: * Second- or third-degree atrioventricular (AV) block * A recent history of strokes * Severe hypotension * Cardiorespiratory instability * Substance abuse * Psychotic illness * Severe dementia
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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
-
Ankara Bilkent City Hospital
Ankara, Çankaya, 06800, Turkey (Türkiye)
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