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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00747981
Other study ID # K 070601
Secondary ID
Status Completed
Phase N/A
First received September 5, 2008
Last updated December 14, 2011
Start date May 2008
Est. completion date October 2011

Study information

Verified date August 2011
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

To access CT Scan as a diagnostic tool for foreign bodies aspiration.


Description:

Comparison with gold standard diagnostic tool, the endoscopy


Recruitment information / eligibility

Status Completed
Enrollment 311
Est. completion date October 2011
Est. primary completion date April 2010
Accepts healthy volunteers No
Gender Both
Age group 6 Months to 16 Years
Eligibility Inclusion Criteria:

- age between 6 months and 16 years

- suspicion of a foreign body aspiration

- health care assurance

- information of parents

Exclusion Criteria:

- emergency situation

- certainly of foreign body presence

- delay for CT Scan realization longer than 24 hours

- no speaking French parents

- parents refusal.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Procedure:
Thoracic CT Scan
Perform a CT Scan and an endoscopy

Locations

Country Name City State
France Paris V University & Assistance Publique Hôpitaux de Paris Paris

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison between CT Scan and endoscopy results 12 HOURS Yes
Secondary X Ray radiation induced by CT Scan TWO YEARS Yes