PERIOPERATIVE MYOCARDIAL DAMAGE IN ROBOT-ASSISTED SURGERY
NCT ID: NCT06502340
Last Updated: 2024-07-18
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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NOT_YET_RECRUITING
63 participants
OBSERVATIONAL
2024-07-15
2024-12-30
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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patient
All patients who will undergo elective robotic-assisted laparoscopic radical prostatectomy
high sensitive troponin I
high-sensitive Troponin I levels
Interventions
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high sensitive troponin I
high-sensitive Troponin I levels
Eligibility Criteria
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Inclusion Criteria
* Patients with I, II, and III according to ASA classification
* Those with body mass index (BMI) below 35kg/m2
* Patients whose consent was obtained before the procedure
Exclusion Criteria
* patients who did not agree to participate in the research
MALE
Yes
Sponsors
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Ankara City Hospital Bilkent
OTHER
Responsible Party
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Betül Güven
assoc. prof
Central Contacts
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Other Identifiers
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E2-23-5211
Identifier Type: -
Identifier Source: org_study_id
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