Diagnostic Errors in Anaphylactic Shock

NCT ID: NCT04825106

Last Updated: 2023-05-11

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

270 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-01-01

Study Completion Date

2022-12-31

Brief Summary

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

Detailed Description

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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

Conditions

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Diagnostic Error

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

SINGLE

Participants

Study Groups

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Expected

Anaphylactic shock occurs after the injection of a drug known to cause allergic reactions

Group Type ACTIVE_COMPARATOR

Diagnostic context

Intervention Type OTHER

A life-threatening situation occurs in 3 different contexts

Unexpected, no distractor

Anaphylactic shock occurs unexpectedly, but their is no medical distractor

Group Type ACTIVE_COMPARATOR

Diagnostic context

Intervention Type OTHER

A life-threatening situation occurs in 3 different contexts

Unexpected, with distractor

Anaphylactic shock occurs unexpectedly. Scenario is set up such, that a tension pneumothorax may be a likely explanation

Group Type ACTIVE_COMPARATOR

Diagnostic context

Intervention Type OTHER

A life-threatening situation occurs in 3 different contexts

Interventions

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Diagnostic context

A life-threatening situation occurs in 3 different contexts

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Physicians taking part in voluntary simulator workshops

Exclusion Criteria

* Refusal to participate or to being videorecorded
Minimum Eligible Age

24 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Basel, Switzerland

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Stephan Marsch

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Basel, Switzerland

Locations

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University Hospital

Basel, Canton of Basel-City, Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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4031-Sim-ANA

Identifier Type: -

Identifier Source: org_study_id

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