Last updated: 11/07/2018 16:42:51
Study Of Perennial Allergic Rhinitis
Clinicaltrials.gov ID
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: Study of Perennial Allergic Rhinitis -Long term treatment study-
Trial description: This study was designed to assess safety of an investigational nasal spray in the treatment of perennial allergic rhinitis. Perennial allergic rhinitis is triggered by house dust, mite and mold etc. Typical symptoms are sneezing, nasal congestion and pruritus and rhinorrhea.
Primary purpose:
Treatment
Trial design:
Single Group Assignment
Masking:
None (Open Label)
Allocation:
Non-randomized
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Enrollment:
65
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Keisuke Masuyama, Yoriko Morioka, Terufumi Hara. Drug Use Investigation on Fluticasone Furoate (Allermist®) 27.5 µg 56 Metered Nasal Spray. Allergol Immunol. 2012;19(12):88-101.
- Inclusion criteria:
- Informed consent.
Inclusion and exclusion criteria
Inclusion criteria:
- Inclusion criteria:
- Informed consent.
- Outpatient.
- Diagnosis of perennial allergic rhinitis with symptoms.
- Able to comply with study procedures. Exclusion criteria:
- Significant concomitant medical condition.
- Use of corticosteroids/allergy medications.
- Laboratory abnormality.
- Positive pregnancy test.
Trial location(s)
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Refer to study documents
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2005-12-10
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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