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Effect of Mupirocin in patients with refractory chronic rhinosinusitis - A prospective, randomised double-blinded controlled trial

Effect of Mupirocin on S.aureus infection in patients with refractory chronic rhinosinusitis - A prospective, randomised double-blinded controlled trial

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000994987
Enrollment
40
Registered
2011-09-19
Start date
2010-01-18
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

We hypothesise that Mupirocin nasal rinses are more efficacious compared to placebo in patients that are bothered by persistent S.aureus infection despite complete sinus surgery.

Interventions

Mupirocin nasal rinses, 0.05% twice daily for 4 weeks.

Sponsors

The Queen Elizabeth Hospital
Lead SponsorHospital

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

Patients with surgically-recalcitrant, S.aureus-positive chronic rhinosinusitis

Exclusion criteria

Mupirocin allergy. Augmentin Duo allergy. Multiple bacterial species on culture. MRSA. Mupirocin-resistant S.aureus.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026