CompletedPhase 4ACTRN12612000162819

Using ketamine (an anesthetic agent) with Propofol (a hypnotic agent commonly used during sedation) during visual examination of large intestine reduces propofol dosage improves the quality of sedation

Propofol in combination with ketamin reduces propofol dosage and improves quality of sedation during colonoscopy: A prospective, randomized and double blind study


Sponsor

Prof. Mehmet Ayhan KUZU

Enrollment

100 participants

Start Date

Sep 20, 2010

Study Type

Interventional

Conditions

Summary

Propofol is frequently used for sedation in endoscopy units. Usually opioids are used in combination to propofol in order to improve the quality of sedation. However combining opioids with propofol usually raises the incidance of adverse events such as apnea. Ketamine is usually used for sedation for invasive procedures outside the operating room especially in children. Its not preffered in adults for sedation because of agitation and hallucinations which can be prevented by using sedative or hypnotic agents. The most important advantage of using ketamine is that it does not supress the airway reflexes. Thus it can be hypotised that ketamine may be a better agent of choice than opioids to combine with propofol during sedation. The aim of this study is to investigate the effects of ketamine added to propofol in terms of propofol sparing effects, quality of sedation, adverse events and recovery times.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This study tests whether adding a low dose of ketamine to propofol during colonoscopy sedation reduces the amount of propofol needed and improves sedation quality. Adults aged 18 and over with ASA I-II status who are undergoing colonoscopy may participate.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Patients were randomized to 2 groups according to applied sedation protocol as follows. Group 1: intravenous bolus saline was administred before propofol Group 2: intravenous bolus 0.25 mg/kg keta

Patients were randomized to 2 groups according to applied sedation protocol as follows. Group 1: intravenous bolus saline was administred before propofol Group 2: intravenous bolus 0.25 mg/kg ketamine was administered before propofol. In each group propofol dosage was titrated according to patients sedation level. For both groups target sedation level was 1-2 with Modified Observer's assessment of Alertness/Sedation Scale.


Locations(1)

Turkey

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ACTRN12612000162819