RSI Observation Follow-up

NCT05775029 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 2300

Last updated 2025-03-07

No results posted yet for this study

Summary

The purpose of this prospective observational study is to determine if compliance to local guildelines for the RSI procedure, after introduction of a RSI-check list, persists over time (36-60months). Any changes in complication rates will also be evaluated.

Conditions

  • RSI
  • Rapid Sequence Induction
  • Complication of Anesthesia
  • Compliant Behavior

Sponsors & Collaborators

  • Jakob Zeuchner

    lead OTHER_GOV

Principal Investigators

  • Michelle Chew, M.D. Ph.D. · Linkoeping University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-05-05
Primary Completion
2025-06-01
Completion
2025-06-01

Countries

  • Sweden

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05775029 on ClinicalTrials.gov