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NCT07816835RecruitingPhase 4

Nebulizer Versus Handheld Maintenance Therapy for Patients With COPD

Source: ClinicalTrials.gov · Last updated 14 Sept 2026

Brief summary (registry, in English)

Multi-site, randomized controlled trial to determine whether patients who report NO symptomatic benefit with their maintenance hand-held inhaler(s), benefit upon switching to nebulized therapy using comparable classes of medications.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
120 (estimated)
First submitted
8 Sept 2026
Start date
14 Jul 2026
Primary completion date
Jun 2027
Lead sponsor
COPD Foundation
Diseases
COPD
NCT number
NCT07816835

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 120
  • From 14 Jul 2026 to the primary completion date, Jun 2027
  • 2 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

  • Current diagnosis of other respiratory disease including asthma, treatment with a LABA/LAMA slow mist inhaler or treatment with SABA/SAMA nebulizer medications 3-4 times per day as maintenance therapy

Other illness

  • Current diagnosis of dementia or known cognitive impairment.
  • Current impairment in manual dexterity (i.e., severe rheumatoid arthritis, severe tremor, etc)

Other

  • Exacerbation of COPD within the last 2 months
  • Current use of daily Prednisone as treatment for COPD

Who the study is looking for

  • \> 10 pack-years smoking cigarettes
  • Diagnosis of COPD based on GOLD Criteria
  • Patients are clinically stable for the past 4 weeks
  • Prior Pulmonary function tests showing FEV1 \< 50% predicted (either 30 minutes post albuterol or within 2-4 hours after using their maintenance long-acting inhaler) within the past 12 months.
  • Currently using a single pMDI or a single DPI with either LABA/LAMA or LABA/LAMA/ICS therapy for at least one month.

Age in the registry: 60 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
Midwest Chest Consultants, P.C.
Coordinator of this site? Confirm its status
Saint CharlesUnited StatesRecruiting
Southeastern Research Center
Coordinator of this site? Confirm its status
Winston-SalemUnited StatesRecruiting

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