- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01066416
Effects of Endoscopic Sinus Surgery for Chronic Sinusitis on Asthma Control
July 19, 2019 updated by: NorthShore University HealthSystem
It is unknown whether surgical treatment of chronic sinusitis improves asthma control in patients with poorly controlled asthma.
This is a randomized trial of surgical plus medical sinus therapy versus medical therapy alone.
Study Overview
Status
Terminated
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
1
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Illinois
-
Evanston, Illinois, United States, 60201
- Evanston Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
Inclusion criteria: General
- 18 years of age or older
- Women need one of the following: negative pregnancy test or suitable birth control or post-menopausal status
- Informed consent and ability to comply with study procedures
- Patients must meet inclusion criteria for both asthma and sinus disease.
Inclusion criteria: Asthma
In order to qualify for the 6 week run-in, patients must have poorly controlled asthma as defined by the following criteria:
- Diagnosis of asthma confirmed either by demonstrating a positive methacholine challenge test (defined as a decrease in FEV1 by at least 20%, following administration of 8mg or less of inhaled methacholine) or a positive bronchodilator response (defined as a change from base line of >12% and at least 200ml in either FEV1 or FVC, following administration of a short-acting, inhaled bronchodilator).
Either:
- Asthma Control Questionnaire score > 1.5 or
- Use of inhaled rescue ß-agonist >/= 16 puffs per week (excluding use as a pre-medication for exercise; 1 nebulizer treatment = 2 puffs of inhaler) at any time during the past month or
- >1 hospitalization or unscheduled MD visit in the past 6 months for asthma symptoms or
- >1 course of oral steroid use in past 6 months or
- > 2 weeks of systemic steroids in last 6 months.
Exclusion Criteria:
- Current smokers or those with at least a 10 pack-year smoking history
- Presence of any concurrent diseases that, in the investigator's opinion, would interfere with participation in the study or that might put the participant at risk
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
PLACEBO_COMPARATOR: Medical therapy
Patients undergo surgery 6 months after randomization
|
Subjects will undergo surgery 6 months after randomization
|
|
EXPERIMENTAL: Surgery
Patients undergo surgery at time of randomization
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
|---|
|
Asthma Control Score
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
July 1, 2009
Primary Completion (ACTUAL)
November 1, 2010
Study Completion (ACTUAL)
December 1, 2010
Study Registration Dates
First Submitted
February 9, 2010
First Submitted That Met QC Criteria
February 9, 2010
First Posted (ESTIMATE)
February 10, 2010
Study Record Updates
Last Update Posted (ACTUAL)
July 23, 2019
Last Update Submitted That Met QC Criteria
July 19, 2019
Last Verified
July 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Immune System Diseases
- Lung Diseases
- Hypersensitivity, Immediate
- Disease Attributes
- Bronchial Diseases
- Otorhinolaryngologic Diseases
- Lung Diseases, Obstructive
- Respiratory Hypersensitivity
- Hypersensitivity
- Paranasal Sinus Diseases
- Nose Diseases
- Asthma
- Sinusitis
- Chronic Disease
Other Study ID Numbers
- 0001 (Researcher)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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