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Completed

NCT Number: NCT01430260

Omnaris Versus Levocetirizine Phase 4 Study

This i a comparison of the efficacy ciclesonide nasal spray and levocetirizine, alone and in combination.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

handok pharmaceuticals co. LTD

Seoul, 135-755, South Korea

About this study

randomized, open-label, three arm, parallel group, multi-center study

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Allergic rhinitis patients aged ≥ 18 years (with a history of AR of 1 years or longer)
  • Moderate to severe patient according to ARIA guideline
  • To have a demonstrated positive skin prick test or other serologic tests to at least 1 allergen.
  • Subjects who complete the subject diary(S) at least 70%.

Exclusion criteria

  • Nasal pathology, including nasal polyps, clinically relevant respiratory tract malformations, recent nasal biopsy (within 60 days), nasal trauma, nasal surgery, atrophic rhinitis, rhinitis medicamentosa (within 60 days), asthma requiring corticosteroid treatment
  • Hypersensitivity to corticosteroid and/or hydroxyzine
  • Hypersensitivity to galactose intolerance, lapp lactase deficiency, glucose-galactose malabsorption
  • A history of respiratory tract infection or disorder within 2 weeks of the screening visit or had a respiratory tract infection during baseline
  • Active asthma requiring treatment with inhaled or systemic corticosteroids and/or routine use of β-agonists
  • Treated with systemic corticosteroids (within 8 weeks of study initiation) or topical corticosteroids (> 1% hydrocortisone, within 4 weeks of study initiation) or antibiotics (within 2 weeks of first visit)

Treatment and study plan

Ciclesonide

Drug

200 ㎍ once daily

Other names: Omnaris

Levocetirizine

Drug

5mg once daily

Other names: XYZAL

Ciclesonide & Levocetirizine

Drug
  • Omnaris (ciclesonide) 200 ㎍ once daily
  • Levocetirizine 5mg once daily

Other names: Omnaris nasal spray, XYZAL

Primary outcomes

  1. rTNSS

    Time frame: 2 weeks

    change from baseline in the average of AM and PM patient assessed reflective TNSS

Secondary outcomes

  1. rTOSS

    Time frame: 2 weeks

    Reflective total ocular symptom sores

  2. TNSS

    Time frame: 2 weeks

    Patient assessed individual TNSS

  3. PANS

    Time frame: 2 weeks

    Physician-assessed overall nasal signs and symptoms severity (PANS)

  4. RQLQ

    Time frame: 2 weeks

    Rhinoconjunctivitis quality of life questionnaire (RQLQ)

Sponsors and collaborators

Lead sponsor

Handok Inc.

Industry

Collaborators

  • Takeda

Registry information

Official study title

A Multi-center, Open, Randomized, Three-arm, Parallel-group, Phase IV Study to Compare the Efficacy of Ciclesonide Nasal Spray and Levocetirizine, Alone and in Combination for the Patient With Allergic Rhinitis

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Sep 8, 2011
Registry last updated
Sep 6, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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