Impact of Respiratory Allergy on Response to Initiation of Biotherapy in Severe Asthma in Adult Severe Asthmatic Patients Followed at Poitiers University Hospital on Biotherapy
IARBASP
1 other identifier
observational
100
1 country
1
Brief Summary
The aim of this study is to take stock of the situation of adult patients with severe asthma on biotherapy, followed up at Poitiers University Hospital, and in particular to increase our knowledge of factors predictive of response to biotherapy. The main aim is to improve the management of adult severe asthma patients treated with biotherapy, according to their allergic status.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Mar 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2024
CompletedFirst Submitted
Initial submission to the registry
March 31, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2025
CompletedFirst Posted
Study publicly available on registry
April 8, 2025
CompletedApril 8, 2025
March 1, 2025
1.1 years
March 31, 2025
March 31, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Find out whether a positive respiratory allergy test influences the efficacy of one or more biotherapies
1 year
Secondary Outcomes (2)
analyze the allergological workup, particularly with regard to common pneumallergens
1 year
look at the response to the biotherapy used
1 year
Study Arms (1)
adult patients with severe asthma on biotherapy
Interventions
analyses in terms of biotherapy and respiratory allergy
Eligibility Criteria
severe asthma patients on dual therapy at POITIERS University Hospital
You may qualify if:
- Severe asthma patient on biotherapy
- Age \> or = 18 years
- Follow-up at Poitiers University Hospital
You may not qualify if:
- Absence of allergological assessment
- Patient's refusal to participate in study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Chu Poitiers
Poitiers, 86000, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 31, 2025
First Posted
April 8, 2025
Study Start
March 1, 2024
Primary Completion
March 31, 2025
Study Completion
March 31, 2025
Last Updated
April 8, 2025
Record last verified: 2025-03