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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02936778
Other study ID # NL52508.078.15
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 2016
Est. completion date April 2019

Study information

Verified date May 2019
Source Erasmus Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will prospectively assess the impact and relevance of several risk factors for children with severe acute asthma (SAA) or acute wheeze that have been identified in retrospective studies. Secondary we will assess short-term medical and psychosocial functioning in patient (and parents) admitted to a PICU for SAA/acute wheeze versus a control group admitted to a MC for SAA/acute wheeze.


Recruitment information / eligibility

Status Completed
Enrollment 221
Est. completion date April 2019
Est. primary completion date April 2019
Accepts healthy volunteers No
Gender All
Age group 2 Years to 18 Years
Eligibility Inclusion Criteria:

- Between 2 and 18 years of age

- Admission to a PICU for SAA or acute wheeze or admission to a MC for SAA or acute wheeze

Exclusion Criteria:

- Patient is outside of specified age range

- Down's Syndrome

- Congenital/acquired heart defect that interferes with normal SAA treatment

- Congenital/acquired airway defect (tracheomalacia/bronchomalacia)

- Primary/secondary immunodeficiency

- Pre-existing chronic pulmonary condition, known to mimic asthma: Cystic Fibrosis, Bronchopulmonary dysplasia, Bronchiolitis obliterans

- If both parents are not able to speak the Dutch language

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Netherlands Erasmus MC Rotterdam Zuid-Holland

Sponsors (12)

Lead Sponsor Collaborator
Erasmus Medical Center Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA), Amphia Hospital, Leiden University Medical Center, Maasstad Hospital, Maastricht University Medical Center, Radboud University, Rijnstate Hospital, Tergooi Hospital, UMC Utrecht, University Medical Center Groningen, VU University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Undertreatment in children admitted to a PICU with a diagnosis of SAA/acute wheeze Undertreatment is defined as: Patient is not using inhaled corticosteroids (ICS), or Patient is using ICS < 7 days (counting from moment of admission to emergency department) according to treatment plan, or Patient is not using ICS according tot treatment plan. Within the time of admission on the PICU/MC, preferably within 48 hours and during follow up after 3-6 months
Secondary Exposure to triggers (single or combined) Pollution/airborne particulate matter (PM10), sensitization/allergen exposure, cigarette smoke exposure (measured by cotinine in urine), presence and type of virus in upper airway tract Within the time of admission on the PICU/MC, preferably within 24 hours
Secondary Socio-economic status Within the time of admission on the PICU/MC
Secondary Frequency of previous asthma-related hospital admissions and/or PICU admissions. Within the time of admission on the PICU/MC and during follow up after 3-6 months
Secondary Severity of disease, defined using the GINA criteria for stepwise management of asthma. Within the time of admission on the PICU/MC, preferably within 48 hours and during follow up after 3-6 months
Secondary Distribution of ADRB2-receptor polymorphisms compared to non-SAA population. Through study completion, preferably within the time of admission on the PICU/MC
See also
  Status Clinical Trial Phase
Completed NCT03493503 - Status Asthmaticus on the PICU; Intravenous Salbutamol Phase 4