Skip to content

Randomized, double-blind, placebo-controlled trial of efficacy of mometasone furoate nasal spray in the initial treatment of Japanese cedar pollinosis

Randomized, double-blind, placebo-controlled trial of efficacy of mometasone furoate nasal spray in the initial treatment of Japanese cedar pollinosis - Efficacy of mometasone in the initial treatment of Japanese cedar pollinosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005986
Enrollment
50
Registered
2011-07-15
Start date
2009-12-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Japanese cedar pollinosis

Interventions

In February 1st, 2010, patients begin to receive mometasone (200 ug per day). This treatment was continued until the end of April for 12 weeks. In February 1st, 2010, patients begin to receive placebo

Sponsors

Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (a) at least two year history of JCCP; (b) sensitization to Japanese cedar pollen assessed by skin prick test; (c) ability to fill in the diary cards accurately

Exclusion criteria

Exclusion criteria: (a) concomitant sinonasal disease affecting the outcomes of this trial (e.g. nasal polyps, rhinosinusitis, nasal septum deviation); (b) concomitant treatment-requiring allergic rhinitis caused by allergens other than Japanese cedar/cypress pollen; (c) rhinitis medicamentosa and non-infectious, non-allergic rhinitis; (d) cedar pollen-specific immunotherapy; (e) sinonasal surgery including laser vaporization of inferior turbinates within 1 year; (f) medication with anti-allergic drugs including antihistamines, chromons, glucocorticoids and decongentants within 2 weeks; (g) hypersensitivity to MFNS; (h) systemic infection including mycosis; (i) pregnancy and breastfeeding

Design outcomes

Primary

MeasureTime frame
Nasal symptom score

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026