NCT03568305

Brief Summary

The general objective of this multicenter, international study is to perform a multivariate descriptive analysis of a large population of well-defined subjects with sensitizer-induced OA ascertained by a positive SIC result in order to provide more information on the characteristics of this condition.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
52

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2017

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2017

Completed
1 year until next milestone

First Submitted

Initial submission to the registry

June 14, 2018

Completed
12 days until next milestone

First Posted

Study publicly available on registry

June 26, 2018

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2019

Completed
Last Updated

June 27, 2018

Status Verified

June 1, 2017

Enrollment Period

2 years

First QC Date

June 14, 2018

Last Update Submit

June 25, 2018

Conditions

Keywords

asthmaoccupational asthma

Outcome Measures

Primary Outcomes (1)

  • Retrospective study to perform a multi-varied descriptive analysis of a cohort of patients with occupational asthma confirmed by a specific inhalation test

    The period from from January 1st, 2006 to December 31st, 2015 will be examined

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patient who performed a specific inhalation test with a positive result between january 2006 and december 2015.- Subject giving their consent for their participation

You may qualify if:

  • Adult Patient
  • Patient who performed a specific inhalation test with a positive result between January 2006 and December 2015.- Subject giving their consent for their participation
  • Patient agreeing to use his data for research purposes

You may not qualify if:

  • Patient objecting to the use of his data for research purposes
  • Subjects under safeguard of justice
  • Subject under guardianship or curatorship

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Service de pneumologie, d'allergologie et de pathologie de l'environnement

Strasbourg, 67091, France

RECRUITING

MeSH Terms

Conditions

Asthma, OccupationalAsthma

Condition Hierarchy (Ancestors)

Bronchial DiseasesRespiratory Tract DiseasesRespiratory HypersensitivityHypersensitivity, ImmediateHypersensitivityImmune System DiseasesOccupational DiseasesLung Diseases, ObstructiveLung Diseases

Study Officials

  • Frédéric De Blay, MD, PhD

    University Hospital, Strasbourg, France

    STUDY DIRECTOR

Central Study Contacts

Frédéric De Blay, MD, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 14, 2018

First Posted

June 26, 2018

Study Start

June 1, 2017

Primary Completion

June 1, 2019

Study Completion

June 1, 2019

Last Updated

June 27, 2018

Record last verified: 2017-06

Locations