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A randomised, cross-over trial of upright sitting with or without positive expiratory pressure during nebulised delivery of medication to improve the pattern of aerosol deposition in healthy participants

Randomised trial of positive expiratory pressure (PEP) to improve deposition in healthy participants

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612000015842
Enrollment
15
Registered
2012-01-04
Start date
2012-03-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Research question: To determine whether the addition of positive expiratory pressure (PEP) improves uniformity of deposition of an inhaled aerosol in upright sitting in healthy participants. Methods: Inclusion criteria: greater than or equal to18 years of age, normal lung function. Participants will inhale a 4mL radioaerosol in two stategies in random order throughout the nebulisation period of 20 minutes: 1. Standard nebulisation period of 20 minutes, or 2. Nebulisation period of 20 minutes with the addition of a PEP device. After each nebulisation a gamma camera will perform a 20-minute deposition scan incorporating a transmission scan to outline the three-dimensional margin of the lung fields. This data will be reconstructed to determine the distribution of the deposited radioaerosol in the lungs. A 15% improvement in uniformity of deposition is the proposed minimum difference that would make further investigation of the PEP strategy worthwhile in patient populations. Significance of project: In many patient populations (eg, cystic fibrosis, HIV and bronchiectasis), the pattern of deposition of inhaled medication is poor and non-uniform. The ability to deliver a drug more uniformly to the lung using the addition of PEP may have a significant impact on treatment efficacy for people with lung disease. Data from healthy participants will aid interpretation of subsequent studies in patients.

Interventions

Participants will inhale 4mL technetium-99m DTPA radioaerosol in random order throughout the nebulisation period of 20 minutes for each of the regimens on two separte days: 1. Standard nebulisation period of 20 minutes, or 2. Nebulisation period of 20 minutes with the addition of a positive expiratory pressure device. The two study days will have a minimum of 48 hours washout between them and not greater than 7 days (to ensure clinical stability). After each nebulisation a gamma camera will perform a 20 minute deposition scan incorporating a transmission scan to outline the three-dimensional margin of the lung fields. This data will be reconstructed to determine the distribution of the deposited radioaerosol in the lungs.

Sponsors

Royal Prince Alfred Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Inclusion Criteria: To participate in this study, a person must: 1 be 18 years of age or older 2 be able to read, write and comprehend English 3 have normal lung function, with greater than or equal to 80% predicted FEV1 4 be willing to inhale a 4mL radioaerosol and undergo a 20-minute gamma scan, on two occasions.

Exclusion criteria

Exclusion Criteria: A person will be ineligible to participate in this study if s/he: 1 has any respiratory condition 2 has significant malignant, neurological or musculoskeletal conditions 3 is unable to perform spirometry reproducibly 4 is pregnant, or is sexually active and unwilling to use contraception during the study

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026