Perioperative Respiratory Support and Postoperative Outcomes
NCT ID: NCT06798883
Last Updated: 2025-01-29
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
1000 participants
OBSERVATIONAL
2025-04-07
2025-05-11
Brief Summary
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Detailed Description
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The "RuVent-A" study will collect data on respiratory support methodologies, initial ventilation parameters, types of surgical interventions, and associated PPC rates in the Russian Federation. This observational study will analyze patient and equipment data across participating centers without altering routine clinical practices.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Russian Federation of Anesthesiologists and Reanimatologists
OTHER
Responsible Party
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Principal Investigators
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Andrey Yaroshetskiy, MD
Role: PRINCIPAL_INVESTIGATOR
Sechenov First Moscow State Medical University
Central Contacts
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Other Identifiers
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FARCT0006
Identifier Type: -
Identifier Source: org_study_id
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