Effects of Omalizumab Compared to Non-Omalizumab Treatment in Asthma Patients

NCT ID: NCT02921178

Last Updated: 2016-10-03

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 124 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2016-09-30
• Study Completion Date: 2017-09-30

Brief Summary

The purpose of this study is effects of Omalizumab compared to non-Omalizumab treatment in the propensity-matched group on asthma exacerbation in asthma patients in Korea: a retrospective cohort in real world.

Omalizumab was approved 2007 in Korea and has been used in this center. We would like to collect and analyze the data and exacerbation outcomes of these patients on Omalizumab; no Korean real world data available.

Detailed Description

1. Primary and secondary outcomes and analysis methods

(1) Primary endpoint Comparison of asthma exacerbation rates of omalizumab-treated vs non-Omalizumab treated group at outcome period (6 months). (asthma exacerbation: at least 1 systemic steroid treatment and/or bursts of systemic oral steroid use by prednisone-equivalent dose ≥45mg/3days, in a 6 month for relieving asthma exacerbations.) Fisher's exact test is examined for asthma exacerbation between omalizumab-treated vs non-Omalizumab treated group.

(2) Secondary endpoint

• Comparison of the clinical parameters Asthma exacerbation rate, ICS sparing effect, OCS requirement, lung function (FEV1%), Healthcare resource use (asthma-related ER visit/hospitalization)

1. Within Omalizumab-treated group between baseline and outcome period

2. Between Omalizumab-treated and not-treated groups at outcome period For comparison of within group, paired T-test and McNemar test are applied for continuous and categorical parameters, respectively. And, T-test and Fisher's exact test are examined for continuous and categorical parameters between Omalizumab-treated and not-treated groups. Incidentally, non-parametric tests will be examined as needed.

• Finding predictor of favorable responders to Omalizumab at 6 months. (Favorable responder: 50% reduction of asthma exacerbation or of steroid requirement during 6 months with/without ICS/LABA) Candidate factors: Omalizumab treatment period/monthly dose, age, gender, asthma treatment duration, total IgE, sputum cell profile, peripheral eosinophilia serum periostin level, anti-asthmatic drug requirements etc.

Binary logistic regression is used for finding predictor of favorable responders. If a serious imbalance of dependent parameter occurs from a low frequency of favorable responder, the descriptive analysis will be applied with T-test and Fisher's exact test.

Conditions

Asthma

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: RETROSPECTIVE

Interventions

Omalizumab

comparision of using Omalizumab and non-Omalizumab treatment

Intervention Type: OTHER

Other Intervention Names

Xolair

Eligibility Criteria

Inclusion Criteria

1. Codes for asthma (ICD-10: J45) dependent on availability

• Who have been diagnosed as having allergic asthma with asthma exacerbations (J45 asthma, J45.0 predominantly allergic asthma and J45.8 mixed asthma)
• Those who initially diagnosed as J45.9 asthma, unspecified, we will refer the evidence of allergic components such as IgE level and skin prick test result.

2. Aged 18-80 years at index date

3. Active asthma, defined as ≥ 1 prescriptions for LABA/ICS during baseline periods

4. un-controlled asthma during the baseline period Any one of three criteria A. Asthma exacerbation B. Asthma-related ER visit/Hospitalization C. Physician defined un-controlled asthma

• Worsening symptom status
• Worsens on tapering of high dose ICS or systemic CS
• Air flow limitation (after appropriate bronchodilator withhold FEV1%<80% predicted)

Exclusion Criteria

• taken biologics during baseline and outcome period

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Ajou University School of Medicine

OTHER

Sponsor Role: lead

Responsible Party

Hae-Sim Park

Ajou University Hospital

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Hae-sim Park, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Ajou University School of Medicine

Other Identifiers

AJIRB-MED-MDB-16-276

Identifier Type: -

Identifier Source: org_study_id