NCT03765307Active, not recruiting
Bronchial Ablation for Treatment of Asthma (BATA) Trial
Safety and Efficacy of the SyMap Bronchial Ablation System for Treatment of Severe Asthma: A Prospective, Multicenter, Randomized Controlled Clinical Trial (Bronchial Ablation for Treatment of Asthma (BATA) Trial)
Source: ClinicalTrials.gov · Last updated 2 Aug 2023
Brief summary (registry, in English)
To evaluate the safety and efficacy of a bronchial radiofrequency ablation system (SyMap Medical (Suzhou) Ltd) in a population of subjects with severe asthma who are still symptomatic despite being managed on high-dose Inhaled Corticosteroids (ICS) and Long-Acting β2-adrenergic Agonists (LABA).
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 160 (actual)
- First submitted
- 2 Dec 2018
- Start date
- 18 Jun 2019
- Primary completion date
- 15 Aug 2024
- Lead sponsor
- SyMap Medical (Suzhou), Ltd.
- Diseases
- Asthma
- NCT number
- NCT03765307
What you commit to
- Study type: Interventional
- Participants enrolled: 160
- From 18 Jun 2019 to the primary completion date, 15 Aug 2024
- 15 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
- More than 4 of oral steroid use for exacerbations of asthma in the past 12 months
- Sensitivity to medications required to perform bronchoscopy (such as lidocaine and benzodiazepines)
- Intubation or admission to the ICU for asthma exacerbations within 2 years prior to treatment
- Previously undergone bronchial thermoplasty
Other illness
- More than 3 lower respiratory tract infections requiring antibiotics in the past 12 months
- Uncontrolled gastroesophageal reflux disease, defined as a significant increase in treatment over the past 6 weeks
- Use of an implantable electrical stimulation device, such as a pacemaker, a cardiac defibrillator or a deep nerve or deep brain stimulator;
- Severe emphysema caused by chronic obstructive pulmonary disease (COPD).
- History of fatal asthma.
- Hemorrhagic or malignant tumors or Coagulopathy.
- Poor compliance judged by the investigator, or other medical conditions that are not suitable for the study
Other
- Pre-bronchodilator Forced Expiratory Volume in one second (FEV1) of less than 45% of predicted.
- 3 or more hospitalizations for exacerbations of asthma in the past 12 months;
- Chronic sinusitis
- Use of systemic immunosuppressants, beta adrenergic blockers, or anticoagulants.
- Uncontrolled obstructive sleep apnea
- Lower bronchial stenosis or distal complete atelectasis or other severe bronchial and pulmonary lesions, as Thoracic spiral CT showed
- Related contraindications for bronchoscopy
- Pregnant, lactating women, or patients with a birth plan in the next year
Who the study is looking for
- Subject is an adult between the ages of 18 to 65 years;
- Diagnosed with asthma who required regular asthma maintenance medication in the past 6 months as follows:
- ICS ≥1000 μg/day beclomethasone or equivalent and LABA ≥1000μg /day salmeterol or equivalent.
- Other medications were allowed, including leukotriene modifiers, and Oral Corticosteroids (OCS) ≤ 10mg/day.
- At least two days of asthma symptoms during 4-weeks of the baseline period.
- Pre-bronchodilator Forced Expiratory Volume in one second (FEV1) of greater than or equal to 45% of predicted.
- Non-smoker (less than 10 pack per year) last for 1 year or greater.
- Baseline AQLQ Score less than or equal to 6.25
- Willingness and ability to comply with the outpatient follow-up.
Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers
Sites (15)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Chinese PLA General Hospital Coordinator of this site? Confirm its status | Beijing | China | Unknown status |
| The First Affiliated Hospital of Guangzhou Medical University Coordinator of this site? Confirm its status | Guangzhou | China | Unknown status |
| The Second Affiliated Hospital Zhejiang University School of Medicine Coordinator of this site? Confirm its status | Hangzhou | China | Unknown status |
| The First Affilated Hospital with Nanjing Medical University Coordinator of this site? Confirm its status | Nanjing | China | Unknown status |
| The Third Affiliated Hospital of Qiqihar Medical University Coordinator of this site? Confirm its status | Qiqihar | China | Unknown status |
| Shanghai Tenth People's Hospital Coordinator of this site? Confirm its status | Shanghai | China | Unknown status |
| Northern Theater Command General Hospital Coordinator of this site? Confirm its status | Shenyang | China | Unknown status |
| University of Chinese Academy of Sciences Shenzhen Hospital Coordinator of this site? Confirm its status | Shenzhen | China | Unknown status |
| Hebei Chest Hospital Coordinator of this site? Confirm its status | Shijiazhuang | China | Unknown status |
| The Second Hospital of Hebei Medical University Coordinator of this site? Confirm its status | Shijiazhuang | China | Unknown status |
| Suzhou Municipal Hospital Coordinator of this site? Confirm its status | Suzhou | China | Unknown status |
| Tangdu Hospital, Second Affiliated Hospital of Air Force Medical University Coordinator of this site? Confirm its status | Xi’an | China | Unknown status |
| The affiliated hospital of xuzhou medical university Coordinator of this site? Confirm its status | Xuzhou | China | Unknown status |
| Northern Jiangsu People's Hospital Coordinator of this site? Confirm its status | Yangzhou | China | Unknown status |
| Yantai Yuhuangding Hospital Coordinator of this site? Confirm its status | Yantai | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.