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Diagnostic Errors in Anaphylactic Shock (ANASim)

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University Hospital Basel

Status

Completed

Conditions

Diagnostic Error

Treatments

Other: Diagnostic context

Study type

Interventional

Funder types

Other

Identifiers

NCT04825106
4031-Sim-ANA

Details and patient eligibility

About

Diagnostic accuracy and quality of management in anaphylactic shock is assessed in three conditions: expected, unexpected with no distractor, unexpected with distractor

Full description

participants: physicians taking part in voluntary workshops. Participants are allocated to teams of three design: prospective, randomized, single-blind setting: simulated anaphylactic shock intervention: participants are allocated to 3 versions of the scenario: 1) expected, 2) unexpected but no distractor, 3) unexpected with distractor

Enrollment

270 patients

Sex

All

Ages

24+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Physicians taking part in voluntary simulator workshops

Exclusion criteria

  • Refusal to participate or to being videorecorded

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

270 participants in 3 patient groups

Expected
Active Comparator group
Description:
Anaphylactic shock occurs after the injection of a drug known to cause allergic reactions
Treatment:
Other: Diagnostic context
Unexpected, no distractor
Active Comparator group
Description:
Anaphylactic shock occurs unexpectedly, but their is no medical distractor
Treatment:
Other: Diagnostic context
Unexpected, with distractor
Active Comparator group
Description:
Anaphylactic shock occurs unexpectedly. Scenario is set up such, that a tension pneumothorax may be a likely explanation
Treatment:
Other: Diagnostic context

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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