Do Preoperative Bilirubin Levels Affect Recovery and Hospital Stay After Sedation Anesthesia?
NCT ID: NCT06849661
Last Updated: 2025-02-27
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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ENROLLING_BY_INVITATION
360 participants
OBSERVATIONAL
2025-01-15
2025-10-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Arm Low Bilirubine Levels
No interventions assigned to this group
Arm High Bilirubine Levels
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* ASA I-IV status
* Both genders
* To be operated under sedation anesthesia for ERCP procedure
Exclusion Criteria
* pregnancy
* lack of informed consent (such as patients with mental retardation or
* language problems)
* history of allergy to any agent used during sedation
* baseline O2 saturation \<90%
* baseline systolic blood pressure \<90 mmHg
* procedure performed under general anesthesia
18 Years
ALL
No
Sponsors
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Naime Yalçın
OTHER
Responsible Party
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Naime Yalçın
Specialist Anesthesiology and Reanimation, Principal Investigator
Locations
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Sağlık Bilimleri Üniversitesi Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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KAEK/2025.01.4
Identifier Type: -
Identifier Source: org_study_id
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