NCT07524543

Brief Summary

To ensure the care of people with severe asthma continues to improve, it is essential we have detailed information on the health and treatment of as many people with the condition as possible. The purpose of the registry is to gather this information and track the progress of patients and how well they are responding to treatment. Medical research using data from the registry will provide a better understanding of asthma and help to develop and improve the care and treatment for patients with asthma. Detailed protocol can be referred to the reference in this trial registration (International severe asthma registry \[ISAR\]: protocol for a global registry).

Trial Health

77
On Track

Trial Health Score

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

Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
127mo left

Started Nov 2025

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress7%
Nov 2025Dec 2036

Study Start

First participant enrolled

November 1, 2025

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

March 28, 2026

Completed
16 days until next milestone

First Posted

Study publicly available on registry

April 13, 2026

Completed
9.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2035

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2036

Last Updated

April 13, 2026

Status Verified

March 1, 2026

Enrollment Period

10.2 years

First QC Date

March 28, 2026

Last Update Submit

April 5, 2026

Conditions

Keywords

Asthma

Outcome Measures

Primary Outcomes (1)

  • Asthma exacerbations

    Number of asthma exacerbations per year

    Every year up to 10 years

Secondary Outcomes (1)

  • Change of medications

    every year up to 10 years

Study Arms (1)

Asthma patients

Severe asthma patients

Eligibility Criteria

Age18 Years - 120 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with severe asthma either 1. on GINA Step 5 therapy 2. Asthma uncontrolled on GINA step 4 therapy (Uncontrolled can be poor symptom control in the past 12 months, persistent airflow limitation in the past 12 months, history of serious exacerbations or history of frequent exacerbations

You may qualify if:

  • Patient with severe asthma with age 18 or over will be recruited.

You may not qualify if:

  • Patients who cannot provide written consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Chinese University of Hong Kong

Hong Kong, Hong Kong

RECRUITING

Related Publications (1)

  • FitzGerald JM, Tran TN, Alacqua M, Altraja A, Backer V, Bjermer L, Bjornsdottir U, Bourdin A, Brusselle G, Bulathsinhala L, Busby J, Canonica GW, Carter V, Chaudhry I, Cho YS, Christoff G, Cosio BG, Costello RW, Eleangovan N, Gibson PG, Heaney LG, Heffler E, Hew M, Hosseini N, Iwanaga T, Jackson DJ, Jones R, Koh MS, Le T, Lehtimaki L, Ludviksdottir D, Maitland-van der Zee AH, Menzies-Gow A, Murray RB, Papadopoulos NG, Perez-de-Llano L, Peters M, Pfeffer PE, Popov TA, Porsbjerg CM, Price CA, Rhee CK, Sadatsafavi M, Tohda Y, Wang E, Wechsler ME, Zangrilli J, Price DB. International severe asthma registry (ISAR): protocol for a global registry. BMC Med Res Methodol. 2020 Aug 14;20(1):212. doi: 10.1186/s12874-020-01065-0.

    PMID: 32819285BACKGROUND

MeSH Terms

Conditions

Asthma

Condition Hierarchy (Ancestors)

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

Central Study Contacts

Wai San Fanny Ko, MD

CONTACT

David Shu Cheong Hui, MD

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Target Duration
10 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Honorary Clinical Professor

Study Record Dates

First Submitted

March 28, 2026

First Posted

April 13, 2026

Study Start

November 1, 2025

Primary Completion (Estimated)

December 31, 2035

Study Completion (Estimated)

December 31, 2036

Last Updated

April 13, 2026

Record last verified: 2026-03

Locations