Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
977 participants
OBSERVATIONAL
2017-02-01
2018-02-08
Brief Summary
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Detailed Description
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After one of the routine sedation protocol used in our department was chosen and applied according to the physical status of the patient and the physicians decision, the datas of the patients will be recruited to the study from the medical records . Patient characteristics (age, gender, weight, height), ASA (American Society of Anethesiology) classification, associated diseases will be recorded . After the procedure was completed all the complications during the 2 hours waiting period in the recovery room will be recorded from the medical records. All the complşcation and recovery times will be recorded from the medical records. Whether the patient received radiocontrast material or not will also be recorded. The patients will be called by phone, and will be questioned for the complications, any epileptic seizure attack, or increase in the number of seizures, any admission to emergency room or any in patient admission to the hospital will be recorded which developed in the first week after the procedure.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Group 1
Epileptic patients who are sedated with a total dose of propofol 2 mg/kg and midazolam 0.1 mg/kg.
No interventions assigned to this group
Group 2
Epileptic patients who are sedated with a total dose of pentothal 4 mg/kg and midazolam 0.1 mg/kg.
No interventions assigned to this group
Group 3
Non-epileptic patients who are sedated with a total dose of propofol 1 mg/kg and ketamine 1 mg/kg.
No interventions assigned to this group
Group 4
Non-epileptic patients who are sedated with a total dose of midazolame 0.1 mg/kg and ketamine 1 mg/kg.
No interventions assigned to this group
Eligibility Criteria
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Exclusion Criteria
ALL
No
Sponsors
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Akdeniz University
OTHER
Responsible Party
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İlker Onguc Aycan
department of anesthesiology and reanimation
Principal Investigators
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Ilker O Aycan, MD
Role: PRINCIPAL_INVESTIGATOR
Akdeniz University Hospital
Locations
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AkdenizU
Antalya, , Turkey (Türkiye)
Countries
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Other Identifiers
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MEDAH
Identifier Type: -
Identifier Source: org_study_id
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