Fact CheckerSign in

NCT07718724Recruiting

Impact of GDMT in Uncontrolled Asthma Patients Receiving MHD Inhaled Corticosteroids + Long-acting β2 Agonist

A Prospective, Multicenter, Cluster-Randomized Trial to Evaluate the Impact of Guideline-Directed Medical Therapy in Uncontrolled Asthma Patients Receiving Medium-to-High Dose Inhaled Corticosteroids Plus Long-acting β2 Agonist

Source: ClinicalTrials.gov · Last updated 24 Sept 2026

Brief summary (registry, in English)

The primary objective of this study is to evaluate whether GDMT can bring significant benefits to disease management in uncontrolled asthma patients receiving medium- to high-dose ICS-LABA. * The intervention period will be up to 48 weeks; * The frequency of follow-up is every 12 weeks.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
540 (estimated)
First submitted
16 Jul 2026
Start date
5 Sept 2026
Primary completion date
30 Apr 2028
Lead sponsor
AstraZeneca
Diseases
Asthma
NCT number
NCT07718724

What you commit to

  • Study type: Interventional
  • Planned participants: 540
  • From 5 Sept 2026 to the primary completion date, 30 Apr 2028
  • 19 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous written diagnosis as "Severe Asthma"; Diagnosis of Severe Asthma includes: severe asthma, or related diagnoses containing "severe asthma", or "bronchial asthma (severe)".
  • Previous use of biologics for asthma treatment;
  • History of respiratory tract infection within 4 weeks prior to Visit 0 (upper respiratory tract infections and lower respiratory tract infections);

Other illness

  • Using systemic glucocorticoids for other diseases;
  • Any significant disease or disorder (e.g., cardiovascular, gastrointestinal, hepatic, renal, neurological, musculoskeletal, endocrine/metabolic, malignant, psychiatric, or significant physical impairment, etc.) which, in the opinion of the investigator, may put the patient at risk because of participation in the study, or may influence the results of the study, or the patient's ability to comply with GDMT.

Other

  • Imaging suggests the presence of bullae or cystic bronchiectasis;
  • Currently participating in other interventional studies;

Who the study is looking for

  • Sign the informed consent form before any study-related procedures;
  • Age 18-75 years (inclusive) at Visit 0;
  • Have a written diagnosis of asthma for more than 6 months prior to Visit 0, and have evidence of reversible airflow limitation prior to Visit 0. Evidence of reversible airflow limitation includes: post-bronchodilator increase in Forced Expiratory Volume in 1 second (FEV1) of ≥12% and an absolute increase of ≥200 mL, or average daily diurnal Peak Expiratory Flow (PEF) variability \>10%, or an increase in FEV1 of ≥12% and an absolute increase of ≥200 mL compared to baseline after 4 weeks of treatment containing ICS, or a positive bronchial provocation test record. If no prior record exists, reversible airflow limitation must be confirmed and documented via a bronchodilator test during Visit 0;
  • Under the usage of MD/HD ICS-LABA;
  • Experienced one or more exacerbations within the past year;
    • Exacerbation is defined as meeting any of the following criteria:
  • Use of systemic corticosteroids (or a temporary increase in the stable dose of baseline oral corticosteroids) for at least 3 days; a single injection of a depot long-acting corticosteroid can be considered equivalent to a 3-day course of systemic corticosteroids;
  • An emergency department or urgent care site visit for asthma (defined as being evaluated and treated in the emergency department or urgent care site for \< 24 hours) requiring the use of systemic corticosteroids for at least 3 days (as described above);
  • Hospitalization for asthma (defined as admission to a hospital and/or being evaluated and treated in a healthcare facility for ≥ 24 hours).

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (19)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
ChengduChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
ChifengChinaRecruiting
-
Coordinator of this site? Confirm its status
DongyangChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
HefeiChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
HengyangChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
HezeChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
JiaxingChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
LangfangChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
MeizhouChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
QuanzhouChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
ShanghaiChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
ShiyanChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
Tai’anChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
ÜrümqiChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
Xi'anChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
YantaiChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
YongzhouChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
YunnanChinaNot yet recruiting
-
Coordinator of this site? Confirm its status
ZhanjiangChinaNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.