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NCT07136025Toboroz

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

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2025. aug. 22. · Több mint 12 hónapja nem frissült - kérdezd meg a helyszínt, nyitott-e még

Következő lépések

Rövid összefoglaló (regiszter, angolul)

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. Identification of potentially modifiable factors affecting prognosis, that is, "treatable characteristics", and individualized bundle management based on these characteristics may help to improve the quality of life of patients with asthma and improve the level of asthma control. Through joint research, this project aims to evaluate the treatable characteristics of asthma in patients with severe asthma in tertiary hospitals across the country, including lung function, fractional exhaled nitric oxide, blood routine, allergen IgE, chest CT, and a detailed questionnaire. The distribution of treatable characteristics of patients with severe asthma and its impact on the quality of life or asthma control level of patients were investigated. For patients with severe asthma, multidisciplinary consultation and shared decision-making were used to establish an individualized bundle management model based on the treatable characteristics of severe asthma. A 6-month randomized parallel controlled clinical trial was conducted to determine whether this model was superior to conventional management in improving the quality of life or asthma control in patients with severe asthma. The implementation of this project will build a new model of individualized management of severe asthma based on treatable characteristics and improve the management level of severe asthma

Állapot (regiszter)
Toboroz
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
200 (tervezett)
Első benyújtás
2025. aug. 18.
Kezdés
2025. febr. 1.
Elsődleges befejezés
2029. jan. 31.
Fő szponzor
Beijing Chao Yang Hospital
Betegségek
Asztma
NCT-szám
NCT07136025

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó
  • Tervezett résztvevők: 200
  • 2025. febr. 1. és az elsődleges befejezés (2029. jan. 31.) között
  • 10 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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Korábbi kezelés

  • 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
  • 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

Más betegség

  • The presence of numerous other lung tissue destructive diseases, such as severe bronchiectasis or pulmonary tuberculosis.
  • Anti-tuberculosis treatment is ongoing

Laborértékek

  • QTc interval prolongation >480ms
  • Taking medications that interact with azithromycin, causing QTc prolongation or existing ECG abnormalities, may lead to arrhythmia

Egyéb

  • Women who are pregnant and lactating

Kiket keres a vizsgálat

  • 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 long-acting β2-receptor antagonists (LABAs), or worsening of symptoms after slight tapering of high-dose therapy.
  • 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

Életkor a regiszterben: 18 év – 80 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (10)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical UniversityBeijingKínaToboroz
China-Japan Friendship HospitalBeijingKínaToboroz
Beijing Tiantan Hospital Affiliated to Capital Medical UniversityBeijingKínaToboroz
The Second Xiangya Hospital of Central South UniversityChangshaKínaToboroz
The First Affiliated Hospital of Guangzhou Medical UniversityGuangzhouKínaToboroz
The Second Affiliated Hospital of Zhejiang University School of MedicineHangzhouKínaToboroz
The First Affiliated Hospital of Guangzhou Medical UniversityShanghaiKínaToboroz
The First Affiliated Hospital of China Medical UniversityShenyangKínaToboroz
Shanxi Bethune HospitalTaiyuanKínaToboroz
Henan Provincial People's HospitalZhengzhouKínaToboroz

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