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NCT02953106: MAN06

Effects of Intranasal Fluticasone Plus Azelastine on Airway Inflammation in Patients With Asthma & Allergic Rhinitis

Terminated Phase 4 Last updated 8 April 2019
What this trial tests

Phase 4 trial testing Azelastine-Fluticasone Nasal in Asthma, Allergic in 7 participants. Terminated before completion.

Timeline
20 January 2017
Primary endpoint
10 September 2018
10 September 2018

Quick facts

Lead sponsorUniversity of Dundee
PhasePhase 4
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingquadruple
Primary purposetreatment
Enrollment7
Start date20 January 2017
Primary completion10 September 2018
Estimated completion10 September 2018
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

University of Dundee

Who can join

18 and older, any sex, with Asthma, Allergic or Rhinitis,Allergic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Single centre, double-blind, placebo controlled, adaptive design, cross-over trial. The primary objective is to assess the additive effects of using combined intranasal fluticasone propionate plus azelastine nasal spray on airway hyperresponsiveness. This is in patients with persistent asthma and allergic rhinitis, receiving inhaled steroid.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Asthma, Allergic

Currently open trials in the same condition.

Other University of Dundee trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02953106.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing