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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

Full criteria on ClinicalTrials.gov

Sites (15)

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

SiteCityCountrySite status
Chinese PLA General Hospital
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BeijingChinaUnknown status
The First Affiliated Hospital of Guangzhou Medical University
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GuangzhouChinaUnknown status
The Second Affiliated Hospital Zhejiang University School of Medicine
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HangzhouChinaUnknown status
The First Affilated Hospital with Nanjing Medical University
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NanjingChinaUnknown status
The Third Affiliated Hospital of Qiqihar Medical University
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QiqiharChinaUnknown status
Shanghai Tenth People's Hospital
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ShanghaiChinaUnknown status
Northern Theater Command General Hospital
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ShenyangChinaUnknown status
University of Chinese Academy of Sciences Shenzhen Hospital
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ShenzhenChinaUnknown status
Hebei Chest Hospital
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ShijiazhuangChinaUnknown status
The Second Hospital of Hebei Medical University
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ShijiazhuangChinaUnknown status
Suzhou Municipal Hospital
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SuzhouChinaUnknown status
Tangdu Hospital, Second Affiliated Hospital of Air Force Medical University
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Xi’anChinaUnknown status
The affiliated hospital of xuzhou medical university
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XuzhouChinaUnknown status
Northern Jiangsu People's Hospital
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YangzhouChinaUnknown status
Yantai Yuhuangding Hospital
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YantaiChinaUnknown status

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