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Bronchoscopic Thermal Saline Ablation (BTSA) of Emphysematous Lung. A New Emphysema Therapy

Lung Volume Reduction in COPD Patients With an Inhomogeneous Severe Emphysema Located in the Upper Lobes, by Injecting Warm Saline Through the Bronchoscope Channel

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01920321
Acronym
BTSA
Enrollment
20
Registered
2013-08-12
Start date
2013-02-28
Completion date
2014-12-31
Last updated
2013-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emphysema

Keywords

COPD, Bronchoscopic LVR, Emphysema, Hot injury

Brief summary

Aim: To evaluate feasibility, safety and efficacy of relatively simple approach of bronchoscopic lung volume reduction (LVR) technology, independent of collateral ventilation. Description: Patients with severe upper lobes heterogeneous emphysema, undergo unilateral bronchoscopic installation of saline thermal energy 50-55 ºC intending to induce an inflammatory airway and parenchymal injury and consequently fibrotic response resulting in LVR;

Detailed description

Inclusion criteria: 1. Age 40-75 unlimited sex. 20 subjects 2. chronic obstructive pulmonary disease (COPD), GOLD 3-4 (global obstructive lung disease). 3. CT scan of lung and included high resolution slices. Demonstrating emphysematous, bullotic changes in the upper lobes. 4. Pulmonary function tests results- total lung capacity(TLC)\>110%, residual volume(RV)\>150%, diffusion of lung CO(DLCO)\<80%,forced expiratory volume 1 second(FEV1):15-45%. 5. 6 minute walking distance (6MWD)\> 140 meters. Exclusion criteria: 1. Active ischemic heart disease, significant arrhythmia. ejection fraction (EF) \<40%. 2. COPD that cause carbon bioxide(CO2) retention above 50 mm Hg and / or oxygen saturation at rest below 88%. 3. Pulmonary hypertension\> 45 mmHg, according to the Echo Test. 4. . Cancer treatment with chemotherapy / radiation or expected life expectancy of less than two years.5. Pregnancy. Methods: . A. Patient preparation and sedation as in diagnostic bronchoscopy. Sedation will be based on midzoln + demerol. The patients will be treated prior the treatment with Inhalation with salbutamol ans ipratropium bromide. Flexible bronchoscope with outer diameter 5 mm is introduced to the targated upper lobe, and placed in wedged position. This is followed by installion of 0.9% natriu, chloride(NaCl) at a temperature of 55ºC exit temperature 50ºC) in portions of 40 ml to 200 ml (in bronchoalveolar lavage up to 300 ml is acceptable. The patient is placed in horizontal position, and continuous ECG blood pressure. Oxygen saturation are monitored. This monitoring will be continue at least 2 hours after treatment. A chest x-ray is followed and the patient remain in the department for overnight. Tracking: Minimum of 6 months - Outpatient follow up include in addition to physical examination extended pulmonary function test and after 3-6 months. low radiation chest CT.

Interventions

Prior the procedure patients undergo - high resolution chest CT , extensive phisiological assessment.

Sponsors

Assaf-Harofeh Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Age 40-75 unlimited sex. 20 subjects 2. COPD, GOLD 3-4 (global obstructive lung disease). 3. CT scan of lung and included high resolution slices. Demonstrating emphysematous, bullotic changes in the upper lobes. 4. Pulmonary function tests results- TLC\> 110%, RV\> 150%, DLCO \<80%,FEV1: 15-45%. 5. 6 minute walking distance \> 140 meters. \-

Exclusion criteria

1. Active ischemic heart disease, significant arrhythmia. Ejection fraction (EF) \<40%. 2. Chronic lung disease that cause CO2 retention above 50 mm Hg and / or oxygen saturation at rest below 88%. 3. Pulmonary hypertension\> 45 mmHg, according to the Echo Test. 4. . Cancer treatment with chemotherapy / radiation or expected life expectancy of less than two years. 5. Pregnancy -

Design outcomes

Primary

MeasureTime frameDescription
Pulmonary function improvemnt6 monthsClinical - COPD assessment test (CAT ) + lung volumes + diffusion capaciry and 6MWD .

Countries

Israel

Contacts

Primary ContactDavid Stav, MD
dstav@asaf.health.gov.il972- 89779024
Backup ContactIsaac Shpirer, MD
972- 89779024

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026