Recruiting NA Asthma

New treatment option for Asthma

Official title The Study About the Identification of Treatable Traits of Severe Asthma and the Construction of Personalized Treatment System

ClinicalTrials.gov ID: NCT07136025

What this study is testing

What it's testing
Severe asthma is a complex and heterogeneous disease. Patients with severe asthma can present with different types of airway inflammation, and are often accompanied by a variety of comorbidities and risk factors.
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 to 80

You may be able to join if

  • Age ≥18 years, and \<80 years with a definite diagnosis of asthma for at least 6 months
  • Patients met the 2024 GINA criteria for severe asthma, which was defined as "uncontrolled" asthma (frequent asthma symptoms, or frequent acute...
  • They were willing to accept multi-disciplinary and multi-dimensional evaluation and signed informed consent
  • Informed consent was obtained and patients were able to participate in the study and 6-month follow-up according to the protocol

You likely can't join if

  • The presence of numerous other lung tissue destructive diseases, such as severe bronchiectasis or pulmonary tuberculosis.
  • Chest surgery or abdominal surgery in the past 3 months
  • Eye surgery had been performed within the past 3 months
  • Myocardial infarction within the previous 3 months
  • Anti-tuberculosis treatment is ongoing
  • Women who are pregnant and lactating
See the full eligibility criteria
Who can join
  • Age ≥18 years, and \<80 years with a definite diagnosis of asthma for at least 6 months
  • Patients met the 2024 GINA criteria for severe asthma, which was defined as "uncontrolled" asthma (frequent asthma symptoms, or frequent acute exacerbations) despite high-dose inhaled corticosteroids (ICS) plus...
  • They were willing to accept multi-disciplinary and multi-dimensional evaluation and signed informed consent
  • Informed consent was obtained and patients were able to participate in the study and 6-month follow-up according to the protocol
What rules you out
  • The presence of numerous other lung tissue destructive diseases, such as severe bronchiectasis or pulmonary tuberculosis.
  • Chest surgery or abdominal surgery in the past 3 months
  • Eye surgery had been performed within the past 3 months
  • Myocardial infarction within the previous 3 months
  • Anti-tuberculosis treatment is ongoing
  • Women who are pregnant and lactating
  • Macrolide use within 4 weeks before the screening period
  • Treatment with anti-ige, anti-IL-5, or anti-IL-5R within 4 weeks before the screening period
  • Inhaled ICS+LABA+ long-acting anticholinergic agent (LAMA) for 4 weeks prior to the screening period 4. Allergy to macrolides
  • QTc interval prolongation \>480ms
  • Taking medications that interact with azithromycin, causing QTc prolongation or existing ECG abnormalities, may lead to arrhythmia

The study team makes the final eligibility decision.

Where it's taking place

  • Beijing, Beijing Municipality, China
  • Guangzhou, Guangdong, China
  • Zhengzhou, Henan, China
  • Changsha, Hunan, China
  • Shenyang, Liaoning, China
  • Shanghai, Shanghai Municipality, China
  • Taiyuan, Shanxi, China
  • Hangzhou, Zhejiang, China

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years to 80 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Beijing, Beijing Municipality, China; Guangzhou, Guangdong, China; Zhengzhou, Henan, China; Changsha, Hunan, China; Shenyang, Liaoning, China; Shanghai, Shanghai Municipality, China and 2 more location(s). Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.