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
Finalized
Finalized
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
Observational study model:
Other
Primary completion date:
Not applicable
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)

No location data available.

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
Finalized
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
Participate in clinical trial
Access to clinical trial data by researchers
Visit website