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
Clinicaltrials.gov ID
Not applicable
EudraCT ID
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EU CT Number
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Trial status
Study complete
Study complete
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:
Enrollment:
1
Primary completion date:
Not applicable
Observational study model:
Other
Time perspective:
Retrospective
Clinical publications:
Not applicable
- 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.
Inclusion and exclusion criteria
Inclusion criteria:
- 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.
Exclusion criteria:
- 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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