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Lycopene supplementation in stable asthma

A placebo-controlled, double-blind, randomised control trial using lycopene-rich supplements to reduce neutrophlic airway inflammation in asthma

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12606000286549
Acronym
DAX
Enrollment
139
Registered
2006-07-07
Start date
2006-07-11
Completion date
2009-02-05
Last updated
2020-04-27

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

Conditions

None listed

Brief summary

This study in asthma examines the ability of lycopene-rich supplements to improve neutrophilic inflammation and disease control, and to reduce exacerbation frequency and severity. It uses a blinded comparison of subjects consuming lycopene-rich supplements versus placebo. It also includes a comparison group of subjects with a high dietary intake of antioxidants.

Interventions

Following a 2 week washout on a low antioxidant diet, subjects receive oral lycopene supplements (45mg/day) for 12 weeks. A comparison group consume a diet high in antioxidants for the duration of the study.

Sponsors

Hunter New England Health Service
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

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

Inclusion criteria

Stable asthma, Non-smokers

Exclusion criteria

Other respiratory disease, Vitamin or mineral use.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026