Management of Pediatric Chronic Rhinosinusitis in Asthmatic Children
Primary Purpose
Chronic Sinusitis, Adenoid Disease - Chronic
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Endoscopic Sinus surgery
Adenoidectomy
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Sinusitis focused on measuring Pediatric, Chronic Sinusitis
Eligibility Criteria
Inclusion Criteria:
- Age 6-12 at time of study enrollment.
- Presence of chronic sinusitis: >90 days 2 or more symptoms of purulent rhinorrhea, nasal obstruction, facial pressure/pain, or cough
- Presence of asthma, as documented in the medical record by the patient's pediatrician and/or pulmonologist
- Failure of medical management of pediatric chronic rhinosinusitis, which current guidelines recommend extended empiric antibiotics for 21 days, which will be either Augmentin or clindamycin in penicillin allergic patients, at standard pediatric weight based dosing. In addition, Flonase nasal spray and nasal saline treatment for three weeks. Failure is considered persistent symptoms despite treatment with the above within the past year.
Exclusion Criteria:
- Previous sinus surgery,
- Previous adenoidectomy, or
- Presence of cystic fibrosis,
- Presence of antrochoanal polyp,
- Immunodeficiency
- Fungal infection.
Sites / Locations
- SUNY Upstate Medical University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Adenoidectomy
Adenoidectomy plus Endoscopic Sinus Surgery
Arm Description
Current standard of care for pediatric chronic rhino sinusitis.
endoscopic sinus surgery in addition to adenoidectomy
Outcomes
Primary Outcome Measures
SN-5 at one year post procedure
A validated tool used to track symptoms of pediatric chronic rhinosinusitis, improvement greater than 0.5
Secondary Outcome Measures
Revision/Alternate procedure, endoscopic sinus surgery
Requirement of the alternate procedure or a revision procedure.
Antibiotic use after surgical procedure
Relapse of chronic rhinosinusitis, if treated with antibiotics will be documented as the number of courses of antibiotics taken for rhino sinusitis in two years after the initial procedure
Complication Rate
Complications associated with medical management, or surgery
Full Information
NCT ID
NCT03336671
First Posted
November 1, 2017
Last Updated
October 5, 2021
Sponsor
State University of New York - Upstate Medical University
1. Study Identification
Unique Protocol Identification Number
NCT03336671
Brief Title
Management of Pediatric Chronic Rhinosinusitis in Asthmatic Children
Official Title
Management of Pediatric Chronic Rhinosinusitis in Asthmatic Children
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Terminated
Why Stopped
Poor recruitment
Study Start Date
July 1, 2017 (Actual)
Primary Completion Date
July 1, 2020 (Actual)
Study Completion Date
July 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
State University of New York - Upstate Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The objectives of this study would be to determine the most effective management for pediatric patients with chronic rhinosinusitis and asthma who fail medical management. The Sinus and Nasal Quality of Life Survey (SN-5), a validated tool, will be used to track symptoms of pediatric chronic rhinosinusitis. A decrease in at least 0.5 is felt to represent an improvement in symptom control. In this study, the SN-5 at one year post intervention will be the primary endpoint. Secondary endpoints include complications, revision surgery, and post operative endoscopy scores.
Detailed Description
Indications for surgery for pediatric chronic rhinosinusitis currently lacks scientific consensus. In general, children who fail medical management are candidates for surgery. Currently, pre-operative evaluation with a CT scan of the sinuses is the gold standard prior to sinus surgery. However, the role of the adenoids and adenoiditis in pediatric chronic sinusitis is incompletely understood. Adenoids may contribute to sinusitis both as a bacterial reservoir and obstruct nasal secretion drainage, owing to their larger relative size in children. Adenoidectomy alone has been found to improve symptoms in 75% of children.
It has been found that 50% of children continued to be symptomatic after adenoidectomy, and went on to require endoscopic sinus surgery (ESS). In addition, of the group that failed, 58% had asthma. Overall, asthma and age have been the only known risk factors for failure of adenoidectomy.
Specific Objectives The objectives of this study would be to determine the most effective management for pediatric patients with chronic rhinosinusitis and asthma who fail medical management. Outcomes will be evaluated using the SN-5, a validated tool used to track symptoms of pediatric chronic rhinosinusitis. A decrease in at least 0.5 is felt to represent an improvement in symptom control. In this study, the SN-5 at one year post intervention will be the primary endpoint. Secondary endpoints include complications, revision surgery, and post operative endoscopy scores.
Study Design
The primary outcome is the SN-5 score one year post surgery. A change of 0.5-1.0 is considered a mild improvement, while a change of at least 1.0 is considered a moderate improvement.
Sixty patients are required to have an 80% chance of detecting, as significant at the 5% level, an increase in the primary outcome measure from 47% in the control group to 80% in the experimental group.
Statistical Methods:
Univariate statistical analysis using chi-square in analysis of binary outcomes. In addition paired t test of preoperative and postoperative SN-5 scores will be performed.
Data Analysis and Interpretation:
Analysis of SN-5, and comparison of Lund-McKay(CT) scores along with post operative endoscopy Kennedy scores.
Study Procedures:
The patient's will initially be seen as a referral to the otolaryngology clinic for symptoms including chronic rhinosinusitis. If they meet inclusion criteria, they will be offered enrollment into the study and consent will be obtained. Their symptoms will be followed at each visit with the SN-5, a validated symptom-scoring tool to evaluate pediatric chronic rhinosinusitis.
If the patient does not improve with medical therapy alone after review of the SN-5 and in discussion with caregivers, he or she will be offered entry into the study, with consent, CT scan of the sinuses, and will be randomized to two different treatment arms. The first is adenoidectomy. The patient will then be followed at defined intervals with evaluation of symptoms by SN-5. Should symptoms worsen or not improve, they will then be offered endoscopic sinus surgery, with findings from the CT scan of the sinuses to guide operative intervention. Adenoidectomy followed by endoscopic sinus surgery is the current standard of care and serves as the control arm. In the other experimental or study arm, the patient will undergo adenoidectomy with endoscopic sinus surgery at the same time. Radioallergosorbent test blood testing for allergies would be performed at the time of surgery in both groups.
For patients who initially improve with medical therapy, but relapse at a later time, they may either undergo consent and randomization if they relapse within a year or a repeat course of medical therapy if it has been one year since previous medical therapy.
Endoscopic sinus surgery, in both arms would be tailored to abnormal findings in the CT scan, as is the standard of care. Radiologists typically examine sinonasal disease of the sinuses, and they would also be requested to comment on the patency of the osteo-meatal unit, as this is a component of the Lund-McKay score. The Lund-McKay score is an objective radiologic grade of the severity of sinusitis. If there is sinus thickening, or narrowing of the osteomeatal unit, endoscopic sinus surgery would be tailored to this using either balloon sinus opening or traditional antrostomy. Patient undergoing endoscopic sinus surgery will likely have at least a maxillary antrostomy and anterior ethmoidectomy performed, with frontal sinusotomy, posterior ethmoidectomy, and sphenoidotomy performed depending on CT or endoscopy findings.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Sinusitis, Adenoid Disease - Chronic
Keywords
Pediatric, Chronic Sinusitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective Randomized Controlled Trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
4 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Adenoidectomy
Arm Type
Active Comparator
Arm Description
Current standard of care for pediatric chronic rhino sinusitis.
Arm Title
Adenoidectomy plus Endoscopic Sinus Surgery
Arm Type
Experimental
Arm Description
endoscopic sinus surgery in addition to adenoidectomy
Intervention Type
Procedure
Intervention Name(s)
Endoscopic Sinus surgery
Other Intervention Name(s)
Functional Endoscopic Sinus Surgery
Intervention Description
Endoscopic sinus surgery would be tailored to abnormal findings in the CT scan, as is the standard of care. Radiologists typically examine sinonasal disease of the sinuses, and they would also be requested to comment on the patency of the osteo-meatal unit, as this is a component of the Lund-McKay score. The Lund-McKay score is an objective radiologic grade of the severity of sinusitis. If there is sinus thickening, or narrowing of the OMU, endoscopic sinus surgery would be tailored to this using either balloon sinuplasty or traditional antrostomy. Patient undergoing endoscopic sinus surgery will likely have at least a maxillary antrostomy and anterior ethmoidectomy performed, with frontal sinusotomy, posterior ethmoidectomy, and sphenoidotomy performed depending on CT or endoscopy findings.
Intervention Type
Procedure
Intervention Name(s)
Adenoidectomy
Intervention Description
Adenoidectomy performed, routine, as a singular procedure not combined with any sinus surgery.
Primary Outcome Measure Information:
Title
SN-5 at one year post procedure
Description
A validated tool used to track symptoms of pediatric chronic rhinosinusitis, improvement greater than 0.5
Time Frame
One year
Secondary Outcome Measure Information:
Title
Revision/Alternate procedure, endoscopic sinus surgery
Description
Requirement of the alternate procedure or a revision procedure.
Time Frame
Two Years
Title
Antibiotic use after surgical procedure
Description
Relapse of chronic rhinosinusitis, if treated with antibiotics will be documented as the number of courses of antibiotics taken for rhino sinusitis in two years after the initial procedure
Time Frame
Two years
Title
Complication Rate
Description
Complications associated with medical management, or surgery
Time Frame
Two Years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Age 6-12 at time of study enrollment.
Presence of chronic sinusitis: >90 days 2 or more symptoms of purulent rhinorrhea, nasal obstruction, facial pressure/pain, or cough
Presence of asthma, as documented in the medical record by the patient's pediatrician and/or pulmonologist
Failure of medical management of pediatric chronic rhinosinusitis, which current guidelines recommend extended empiric antibiotics for 21 days, which will be either Augmentin or clindamycin in penicillin allergic patients, at standard pediatric weight based dosing. In addition, Flonase nasal spray and nasal saline treatment for three weeks. Failure is considered persistent symptoms despite treatment with the above within the past year.
Exclusion Criteria:
Previous sinus surgery,
Previous adenoidectomy, or
Presence of cystic fibrosis,
Presence of antrochoanal polyp,
Immunodeficiency
Fungal infection.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Haidy Marzouk, MD
Organizational Affiliation
State University of New York - Upstate Medical University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mark Arnold, MD
Organizational Affiliation
315 464-4678
Official's Role
Study Director
Facility Information:
Facility Name
SUNY Upstate Medical University
City
Syracuse
State/Province
New York
ZIP/Postal Code
13202
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Management of Pediatric Chronic Rhinosinusitis in Asthmatic Children
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