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N/A N=8,790

Retrospective Record Review of Adults and Children Advised for Allergen Immunotherapy (MK-7243-022)

Perennial Allergic Rhinitis · Seasonal Allergic Rhinitis

Enrolled (actual)
8,790
Serious AEs
Results posted
Mar 2014
Primary outcome: Primary: Percentage of Participants Advised to Start AIT Who Elected Subcutaneous Immunotherapy (SCIT) Shots or Sublingual Immunotherapy (SLIT) Drops — 28.2; 8.0 percentage of participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
ALK-Abelló A/S
Primary completion
May 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants Advised to Start AIT Who Elected Subcutaneous Immunotherapy (SCIT) Shots or Sublingual Immunotherapy (SLIT) Drops
28.2; 8.0
PRIMARY
Percentage of Participants Who Initiated SCIT or SLIT and Completed 5 Years of Treatment
10.8; 2.6
PRIMARY
Duration of Treatment With SCIT or SLIT
2.4; 1.9
PRIMARY
Reason for Discontinuation of SCIT or SLIT More Than 6 Months Before Completion of the Recommended Course
67; 69; 7; 4; 1; 3
SECONDARY
Percentage of Participants With a Co-morbidity of Asthma Who Initiated SCIT or SLIT
25.2; 8.7
SECONDARY
Duration of SCIT or SLIT Treatment for Participants With AR and Asthma or AR Alone
2.4; 2.4; 2.1; 1.8

Summary

The purpose of this study is to determine the proportion of participants that initiate allergen immunotherapy (AIT) upon the recommendation of their physician and the proportion of participants that persist with their AIT throughout the recommended course.

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of AR with or without allergic conjunctivitis (AC)
  • Documented provider-to-patient or parent discussion of AIT as a treatment option

Exclusion Criteria

  • Participants receiving AIT as an AR treatment without documented provider-to-patient or parent discussion of AIT as a treatment option
  • Participants receiving immunotherapy for insect sensitivities only
  • AIT started before 2005
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01549340). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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