Last updated: 11/03/2018 20:53:21

Evaluation of clinical and economic benefits of fluticasone furoate compared with mometasone furoate and budesonide in the treatment of allergic rhinitis

GSK study ID
200600
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Evaluation of clinical and economic benefits of fluticasone furoate compared with mometasone furoate and budesonide in the treatment of allergic rhinitis
Trial description: Objectives: To calculate the cost-effectiveness reason and the incremental cost effectiveness ratio for the treatment of allergic rhinitis (AR) using fluticasone furoate compared with mometasone furoate and budesonide. Methods: we developed a cost-effectiveness analysis by mean a Markov model and we developed a meta-analysis for fluticasone furoate and other for mometasone about improve the symptoms of AR using the TOSS scale, for budesonide we used the only one study published in the literature. We calculate number of reports in percent about improves patient’s symptoms, and these results were used like inputs. We made a probabilistic sensitivity analysis. The time horizon was during 12 months. All the costs are expressed in Mexican currency Results: The effectiveness measured by improving of ocular symptoms of AR was superior in the fluticasone group (60.21%) then mometasone (47.95%) and in the end budesonida (28.00%). The annual cost was lower for fluticasone ($6,036), followed by mometasona ($7,962) and the most expensive was budesonide ($10,028), so mometasone and budesonide are dominated by fluticasone. The fluticasone’s efficay was superior to mometasone and budesonida (12.26%) and (32.21%) respectively. The probabilistic analysis cost-effectiveness shows the most of the results are in the quadrant lower cost and more effectiveness (85.9% vs mometasone and 97.5% vs budesonida). Conclusions: To use fluticasone in the treatment of AR is an option more effective with a lower cost for the treatment of AR.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:

percent about improves patient’s symptoms

Timeframe: 12 months

Secondary outcomes:
Not applicable
Interventions:
  • Drug: budesonide
  • Drug: Mometasone furoate
  • Drug: Fluticasone furoate
  • Enrollment:
    1
    Primary completion date:
    Not applicable
    Observational study model:
    Other
    Time perspective:
    Retrospective
    Clinical publications:
    Not applicable
    Medical condition
    Rhinitis, Allergic, Perennial
    Product
    GSK1004723, fluticasone furoate, fluticasone furoate/GSK1004723
    Collaborators
    Not applicable
    Study date(s)
    March 2011 to May 2011
    Type
    Observational
    Phase
    Not applicable

    Participation criteria

    Sex
    Female & Male
    Age
    2 - 75 Year
    Accepts healthy volunteers
    none
    • The cost minimization analysis and budgetary impact, patients with 2 or more years were considered for the evaluation.
    • For the cost- effectiveness analysis, patients with 12 or more years old were considered during the evaluation.
    • Patients with asthma treated with corticosteroids.

    Trial location(s)

    This study does not involve prospective enrollment of participants.

    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
    2011-23-05

    Plain language summaries

    Not applicable. GSK’s transparency policy provides for Plain Language Summaries for Interventional studies.

    Additional information about the trial

    Not applicable
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