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Effectiveness of zinc supplementation as an adjunct therapy in managing idiopathic pulmonary fibrosis

Evaluating the effect of zinc supplementation on lung function in idiopathic pulmonary fibrosis: RCT

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624001171505
Enrollment
130
Registered
2024-09-25
Start date
2025-06-02
Completion date
2027-07-30
Last updated
2024-09-30

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

Conditions

None listed

Brief summary

The proposed study investigates zinc's impact on lung function, IPF-related complications including pulmonary hypertension, and acute exacerbation in IPF. The findings will establish a rationale for incorporating zinc into IPF management and lay the foundation for further research into zinc status monitoring in existing IPF care protocols.

Interventions

Zinc gluconate, 30 mg will be administered as a daily oral tablet for 12 months. Adherence will be monitored through tablet returns, where participants will be given a bottle each month, and the remaining pills will be counted at each visit to assess compliance with the treatment regimen.

Sponsors

University of Adelaide
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

Patients 40 years of age or older who have received a diagnosis of IPF according to 2022 international guidelines and confirmed by a multidisciplinary team.

Exclusion criteria

IPF patients with severe co-existing medical conditions as determined by the investigators such as but not limited to advanced cardiovascular diseases, uncontrolled diabetes, or malignancies.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026