Study of Chronic Rhinosinusitis Symptoms in Asthma Patients Undergoing Treatment With Reslizumab

NCT ID: NCT03369574

Last Updated: 2019-11-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2017-11-14

Study Completion Date

2018-10-19

Brief Summary

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The primary objective of this research is to monitor chronic rhinosinusitis (CRS) symptoms in asthma patients who are undergoing treatment with reslizumab. A secondary objective is to explore whether there are sub-populations that appear to benefit or not benefit from reslizumab in terms of their CRS symptoms.

Detailed Description

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This is a prospective observational study of patients receiving reslizumab to treat their asthma. Some asthma patients receiving reslizumab also have CRS, which might also be improved by this drug. Study measures will be obtained from the medical records of eligible subjects who consent to participate. The study has no specific procedures per se, because all study measures are acquired during the course of standard of care treatment and will be abstracted from those medical records.

Conditions

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Chronic Rhinosinusitis (Diagnosis) Asthma Nasal Polyps

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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chronic rhinosinusitis and eosinophilic asthma

Adults over the age of 18, diagnosed with poorly controlled moderate to severe asthma with an eosinophilic phenotype (defined by blood eosinophil count of 150 µL or greater within 6 weeks of enrollment) who are initiating/undergoing reslizumab therapy and also carry a physician diagnosis of chronic rhinosinusitis with nasal polyposis

Reslizumab

Intervention Type DRUG

reslizumab administration

Interventions

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Reslizumab

reslizumab administration

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Age is 18 years or older
* Physician diagnosis of poorly controlled moderate to severe asthma despite typical medical therapy with an eosinophilic phenotype (defined by blood eosinophil count of 150 µL or greater within 6 weeks of enrollment)
* Initiating or undergoing reslizumab therapy (Reslizumab - Patient Information listed in Appendix 1 for reference)
* Physician diagnosis of chronic rhinosinusitis with nasal polyposis
* Able to understand and willing to provide informed consent
* Able to complete standard of care English-language questionnaires

Exclusion Criteria

* Current smokers
* Significant uncontrolled medical conditions
* Ongoing malignancy or history of cancer in remission for less than 12 months
* Subjects who had received immunosuppressive medications within 3 months of enrollment
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Rochester

OTHER

Sponsor Role lead

Responsible Party

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Li-Xing Man

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Li-Xing Man, MSc, MD, MPA

Role: PRINCIPAL_INVESTIGATOR

University of Rochester

Locations

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University of Rochester Department of Otolaryngology Head and Neck Surgery

Rochester, New York, United States

Site Status

Countries

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United States

References

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Other Identifiers

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RSRB 60712

Identifier Type: -

Identifier Source: org_study_id

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