An Evaluation of the AeriSeal System for CONVERTing Collateral Ventilation Status in Patients With Severe Emphysema
An Evaluation of the AeriSeal System for CONVERTing Collateral Ventilation Status in Patients With Severe Emphysema: The CONVERT II Trial
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 40 Years to 80 Years
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
- Time periods mentioned: 24 months
Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.
Show the study's own words
- "Subjects with CV- status will then undergo placement of Zephyr Valve in the target lobe for bronchoscopic lung volume reduction (BLVR) and be followed for 24 months."
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study tests whether AeriSeal Foam can stop air from passing between lung sections through unwanted paths. It is for adults ages 40–80 with severe emphysema, a lung disease, that affects some lung sections more than others. People whose unwanted airflow stops will receive Zephyr Valves to reduce lung volume and have follow-up visits for 24 months.
This is a prospective, open-label, multi-center, single-arm study planned to enroll 200 subjects with heterogeneous emphysema and collateral ventilation (CV) in the target lobe. Subjects will undergo instillation of AeriSeal Foam in the target lobe and subsequent assessment of CV status using Chartis Pulmonary Assessment System. Subjects with CV- status will then undergo placement of Zephyr Valve in the target lobe for bronchoscopic lung volume reduction (BLVR) and be followed for 24 months.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- Be 40–80 years old, agree to join, and be able to take part.
- Have finished a lung rehab program in the past 12 months.
- Have stopped smoking for at least 8 weeks before signing the consent form, confirmed by a test.
- Have a recent CT lung scan showing uneven emphysema damage and gaps between lung sections that meet the study’s rules.
- Have unwanted airflow between lung sections, confirmed by the Chartis test.
- Be able to walk 150–450 meters in 6 minutes and have shortness of breath that meets the study’s limits.
- Meet the study’s breathing test limits for airflow, trapped air, lung size, and oxygen transfer.
- Have recommended vaccines against lung infections, including COVID-19, and have been on the best medical treatment for over a month.
Who can't join
- Certain past lung surgeries, transplants, airway stents, or lung volume treatments. A limited exception applies to past Zephyr Valve treatment.
- Certain lung scan problems, including concerning spots, infection, damage after COVID-19, or very large air pockets.
- Three or more hospital stays for COPD flare-ups in the past year, or one in the past 8 weeks; asthma or mucus-heavy chronic bronchitis as the main illness; or serious damage that widens the airways.
- Need a breathing machine through a tube, have severely abnormal blood oxygen or carbon dioxide levels, or high blood pressure in the lungs. CPAP or BiPAP for sleep apnea is allowed.
- Certain serious heart, kidney, blood, or other illnesses; a recent stroke; fainting during exercise that is not controlled; or a known inherited lack of the lung-protecting protein alpha-1 antitrypsin.
- Cannot take needed medicines or pause certain blood thinners; have relevant medicine or device allergies; or recently used high-dose steroid pills or medicines that weaken the immune system.
- Are pregnant, breastfeeding, or planning pregnancy within 12 months; or have a body mass index, a weight-to-height measure, below 18 or above 35.
- Recently joined certain studies of unapproved treatments, or have another condition that the study doctor believes makes joining unsafe or follow-up difficult.
Simplified for readability. The official criteria below are what the study team uses.
Official eligibility criteria
Inclusion Criteria: 1. Subject is willing and able to provide informed consent and to participate in the study. 2. Subject is aged ≥ 40 and ≤ 80 years at the time of the ICF signature date. 3. Subject has completed a documented pulmonary rehabilitation (in clinic or home-based) program within 12 months prior to Baseline. 4. Subject has stopped smoking for at least 8 weeks prior to the ICF signature date as confirmed by carboxyhemoglobin or cotinine levels. 5. Subject has a recent HRCT meeting the scan parameter requirements and performed within 3 months of the ICF signature date with the following findings at -910 Hounsfield Units: 1. At least one (1) lobe with segmental emphysema destruction score ≥ 50%. 2. Subject has heterogenous emphysema, defined as difference in emphysema destruction score of ≥ 15 between the density scores of the target lobe and the ipsilateral non-target lobe(s) per QCT report with % voxel density of \< -910 HU. For non-target lobes that include the RML, calculate the combination of non-target lobes as a single density score using volume-weighted percent. 3. LUL, LLL, RUL, RLL, or RUL+RML are targets for valve intervention. 4. Subject has a gap in the interlobar fissure that corresponds to one or more segments and the fissure(s) contacting the target lobe is ≥ 80% complete per QCT report. 5. Subject has 98% of the fissure gap confined to a maximum of 3 segments within the target lobe per Fissure Targeting Report (FTR). 6. Subject has 6MWD ≥ 150 m and ≤ 450 m. 7. Subject has clinically significant dyspnea with an mMRC score of ≥ 2. 8. Subject has post-bronchodilation FEV1 ≥ 15% predicted and ≤ 45% predicted. 9. Subject has an FEV1/FVC ratio of \< 0.7. 10. Subject has post-bronchodilation TLC, measured by body plethysmography, ≥ 100% predicted. 11. Subject has post-bronchodilation RV ≥ 175% predicted, measured by body plethysmography. 12. Subject has post-bronchodilation DLCO ≥ 20% predicted. 13. Subject has received preventative vaccinations against potential respiratory infections, including COVID-19, consistent with local recommendation or policy. 14. Subject is on optimal medical management for more than one month prior to the ICF signature date. 15. Subject has collateral ventilation (CV+) as confirmed per the Chartis assessment prior to the AeriSeal Index Procedure. Exclusion Criteria: 1. Subject has prior lung volume reduction surgery, lobectomy or pneumonectomy, lung transplantation, airway stent placement, pleurodesis, or BLVR of any type, except BLVR using Zephyr Valve with \< 50% TLVR at 6 months, followed by valve removal \> 6 months prior to ICF signature date. 2. Subject has visible radiological abnormality on HRCT scan such as pulmonary nodule greater than 0.8 cm in diameter (does not apply, if present for 2 years or more without increase in size or if deemed benign by biopsy) or active pulmonary infection (e.g., unexplained parenchymal infiltrate, significant interstitial lung disease or significant pleural disease). 3. Post-COVID-19 pathology on CT, including ground glass opacities with or without consolidation, adjacent pleura thickening, interlobular septal thickening, or air bronchograms. 4. Large bullae encompassing greater than 1/3 of the total lung. 5. Subject had 3 or more COPD exacerbations requiring hospitalization within 12 months preceding the ICF signature date or a COPD exacerbation requiring hospitalization within 8 weeks of the ICF signature date. Subjects may be re-considered for future enrollment. 6. Subject has asthma as their primary diagnosis. 7. Subject has chronic bronchitis (defined as greater than 4 tablespoons of sputum production per day) as their primary diagnosis. 8. Subject has clinically significant bronchiectasis. 9. Subjects with evidence of active respiratory infection should be considered for enrollment only after satisfactory resolution. 10. Subject requires invasive ventilatory support. Note: The use of Continuous Positive Airway Pressure (CPAP) or BiPAP devices for sleep apnea is permitted. 11. Subject has severe gas exchange abnormalities as defined by any one of the following tests, conducted at rest, on room air, as tolerated. * PaCO2 ≥ 50 mm Hg (6.7 kPa) * PaO2 \< 45 mm Hg (6.0 kPa) 12. Subject has pulmonary hypertension, defined as mean pulmonary systolic pressure \> 45 mm Hg. 13. Subject has known documented alpha-1 antitrypsin deficiency. 14. Subject has clinically significant hematological disorder. 15. Subject has recent significant unplanned or unexplained weight loss or other relevant comorbidities considered by the investigator to be potentially confounding or limiting to the subject's participation in the study. 16. Subject has non-atrial arrhythmias or conduction abnormalities on EKG. 17. Subject has high cardiac risk after undergoing cardiac risk assessment in accordance with published guidelines (Fleisher 2007) or has ischemic heart disease, congestive heart failure, cerebrovascular disease (stroke or TIA within 6 months of the ICF signature date), serum creatinine \> 2.0 mg/dL (177 μmol/L), or left ventricular ejection fraction (LVEF) \< 45% on echocardiogram. 18. Subject has uncontrolled exercise induced syncope. 19. Subject has evidence of severe disease which in the judgment of the investigator may compromise the anticipated treatment effect or the subject's survival for the duration of at least 12 months. 20. Subject has any other condition that the investigator believes would interfere with the intent of the study or would make participation not in the best interest of the subject including but not limited to alcoholism, high risk for drug abuse, or noncompliance in returning for follow-up visits. 21. Subject cannot tolerate corticosteroids or relevant antibiotics. 22. Subject use of systemic corticosteroids \> 20 mg/day prednisolone or equivalent within four (4) weeks of the ICF signature date. Subjects may be re-considered for future enrollment. 23. Subject use of immunosuppressive agents within four (4) weeks of the ICF signature date. Subjects may be re-considered for future enrollment. 24. Subject is unable to temporarily discontinue heparins and oral anticoagulants (e.g., warfarin, dicumarol) according to local pre-procedural protocols. Note: Antiplatelet drugs including aspirin, thienopyridines and ticagrelor are permitted. 25. Subject has allergy or sensitivity to medications required to safely perform bronchoscopy under conscious sedation or general anesthesia. 26. Subject has known allergy to the following device components: Polyether block amide (PEBAX), Polyvinyl Alcohol or Glutaraldehyde, Nitinol (nickel-titanium) or its constituent metals (nickel or titanium) or Silicone. 27. Subject is a female who is pregnant (positive βHCG Pregnancy test), breast-feeding, or planning to be pregnant in the next 12 months. 28. Subject has Body Mass Index \< 18 kg/m2 or \> 35 kg/m2. 29. Subject participated in an investigational study of a drug, biologic, or device not currently approved for marketing within 30 days prior to the ICF signature date. Note: Subjects being followed as part of a long-term surveillance of a non-pulmonary study that has reached its primary endpoint are eligible for participation in this study.
Study sites (20)
AZ
- Banner University Medical Center · Phoenix, AZ 85006Maria Masters · Study contact · 602-827-2363 · mlmasters@arizona.eduRaed Alalawi, MD · Study contact · raed.alalawi@bannerhealth.eduRaed Alalawi, MD · Principal investigatorMore trials in Phoenix
CO
- UCHealth - Medical Center of the Rockies · Loveland, CO 80538Abby Dowling · Study contact · 970-624-1580 · Abby.Dowling@uchealth.orgKirk DePriest, MD · Study contact · Kirk.DePriest@uchealth.orgKirk DePriest, MD · Principal investigatorMore trials in Loveland
CT
- Saint Francis Hospital and Medical Center (Trinity Health of New England) · Hartford, CT 06105Kendra Williams · Study contact · 860-714-7161 · KLWillia@TrinityHealthOfNE.orgAmber Newman · Study contact · 860-714-4055 · Amber.Newman@TrinityHealthOfNE.orgAnil Magge, MD · Principal investigatorMore trials in Hartford
FL
- Orlando Health · Orlando, FL 32806Donya Shahnavaz · Study contact · 321-841-7303 · donya.shahnavaz@orlandohealth.comMark Vollenweider, MD · Study contact · Mark.Vollenweider@orlandohealth.comMark Vollenweider, MD · Principal investigatorMore trials in Orlando
IL
- Northwestern University · Chicago, IL 60611Adriana Martinez · Study contact · 312-926-6680 · adriana.martinez@northwestern.eduMomen Wahidi, MD · Study contact · momen.wahidi@nm.orgMomen Wahidi, MD · Principal investigatorMore trials in Chicago
- University of Chicago Medical Center · Chicago, IL 60637Jessica Tuck · Study contact · 773-795-4434 · Jessica.Tuck@bsd.uchicago.eduAjay Wagh, MD · Study contact · awagh@bsd.uchicago.eduAjay Wagh, MD · Principal investigatorMore trials in Chicago
- OSF Saint Francis Medical Center · Peoria, IL 61606Kimberly Hartwig · Study contact · 309-655-4229 · kimberly.hartwig@osfhealthcare.orgPatrick Whitten, MD · Study contact · patrick.e.whitten@osfhealthcare.orgPatrick Whitten, MD · Principal investigatorMore trials in Peoria
KY
- University of Kentucky · Lexington, KY 40536Srushan Shankara Bhaktula · Study contact · 859-562-0882 · srushan.bhaktula@uky.eduAshish Maskey, MD · Study contact · ashish.maskey@uky.eduAshish Maskey, MD · Principal investigatorMore trials in Lexington
MA
- Beth Israel Deaconess Medical Center · Boston, MA 02115Maria Lopez Giron · Study contact · 786-967-8448 · mlopezgi@bidmc.harvard.eduAdnan Majid, MD · Study contact · amajid@bidmc.harvard.eduAdnan Majid, MD · Principal investigatorMore trials in Boston
- Brigham Lung Center · Boston, MA 02115More trials in Boston
MI
- Henry Ford Hospital · Detroit, MI 48202Ruth George · Study contact · 313-916-1791 · rgeorg11@hfhs.orgAvi Cohen · Study contact · acohen4@hfhs.orgAvi Cohen, MD · Principal investigatorMore trials in Detroit
OH
- Cleveland VA Northeast · Cleveland, OH 44106More trials in Cleveland
PA
- Penn Medicine · Philadelphia, PA 19107Katelyn Lobo · Study contact · 215-615-0132 · katelyn.lobo@pennmedicine.upenn.eduKevin Ma, MD · Study contact · kevin.ma@pennmedicine.upenn.eduKevin Ma, MD · Principal investigatorMore trials in Philadelphia
- Temple University · Philadelphia, PA 19140Helga Criner · Study contact · 215-707-1559 · Lii-Yoong.Criner@tuhs.temple.eduGerard Criner · Study contact · gerard.criner@tuhs.temple.eduGerard Criner, MD · Principal investigatorMore trials in Philadelphia
- Allegheny General Hospital · Pittsburgh, PA 15212Paige Rutter · Study contact · 412-295-7659 · paige.rutter@ahn.orgStephanie Baltaji, MD · Study contact · Stephanie.Baltaji@ahn.orgStephanie Baltaji, MD · Principal investigatorMore trials in Pittsburgh
- University of Pittsburgh Medical Center (UPMC) · Pittsburgh, PA 15213Paula Consolaro · Study contact · 412-605-1904 · consolaropj@upmc.eduFrank Sciurba, MD · Study contact · sciurbafc@upmc.eduFrank Sciurba, MD · Principal investigatorMore trials in Pittsburgh
TN
- Fort Sanders Regional Medical Center (StatCare) · Knoxville, TN 37916Jennifer Thornton · Study contact · 865-588-8831 · jthornton@statcaremed.netVarun Shah, MD · Study contact · vshah@statcaremed.netVarun Shah, MD · Principal investigatorMore trials in Knoxville
TX
- University of Texas Southwestern · Dallas, TX 75235Khyati Vadera · Study contact · 214-645-8464 · khyati.vadera@utsouthwestern.eduMuhanned Abu-Hijleh, MD · Study contact · muhanned.abu-hijleh@utsouthwestern.eduMuhanned Abu-Hijleh, MD · Principal investigatorMore trials in Dallas
VA
- Inova Fairfax Hospital · Falls Church, VA 22042Alma Khan · Study contact · 703-776-5912 · alma.khan2@inova.orgPriya Patel, MD · Study contact · priya.patel2@inova.orgPriya Patel, MD · Principal investigatorMore trials in Falls Church
WI
- Medical College of Wisconsin (MCW) · Milwaukee, WI 53226Alexandra Cook · Study contact · 414-955-6839 · alcook@mcw.eduJonathan Kurman, MD · Study contact · jkurman@mcw.eduJonathan Kurman, MD · Principal investigatorMore trials in Milwaukee