- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05724290
Mechanism of EGR2 in Allergic Rhinitis
February 9, 2023 updated by: Zu-xia Ma
The Regulatory Mechanism of EGR2 Mediated by miR-150-5p on Allergic Rhinitis
EGR2 may be a target for the treatment of nasal polyps.
Study Overview
Detailed Description
There is much debate about the etiology of nasal polyps, so the pathogenesis of nasal polyps still needs to be clarified.
Surgery for noninflammatory nasal polyps may be better control, but surgery is not effective for recurrent sinusitis and nasal polyps.
Therefore, more research is needed to determine the best targeted therapy for nasal polyps.
We found that EGR2 expression was upregulated in CRSwNP patients with allergic rhinitis.In addition, the expression of EGR2 in CRSwNP mucosa was significantly higher than that in the control group, and the expression of EGR2 in CRSwNP with allergic rhinitis was higher than that in CRSwNP without allergic rhinitis.
EGR2 may be involved in the pathogenesis of nasal polyps, and may also be related to the severity and recurrence of nasal polyps.
EGR2 may be a target for the treatment of nasal polyps.
Study Type
Interventional
Enrollment (Anticipated)
3
Phase
- Phase 1
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
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Zunyi, China, 563003
- Department of Central Laboratory of the Third Affiliated Hospital of ZunYi Medical University
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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
16 years to 76 years (ADULT, OLDER_ADULT, CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
All patients were stopped by systemic or topical corticosteroid treatment at least one month before the study.
Exclusion Criteria:
Patients had NPs accompanied by choanal polyps, fungal nasal sinusitis, cystic fibrosis, acute upper airway upper infection or other systemic diseases.
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: BASIC_SCIENCE
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: TRIPLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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EXPERIMENTAL: immunohistochemistry
Thirty-eight patients with confirmed nasal polyps (20 with primary CRSwNP and allergic rhinitis (AR) and 18 with CRSWNP) and 20 patients with chronic hypertrophic rhinitis were included.
The nasal polyps and mucosal specimens of all patients were collected and analyzed by immunohistochemistry
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We investigated the expression of EGR2 in patients with nasal polyps through immunohistochemistry.
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EXPERIMENTAL: WestBlot
Thirty-eight patients with confirmed nasal polyps (20 with primary CRSwNP and allergic rhinitis (AR) and 18 with CRSWNP) and 20 patients with chronic hypertrophic rhinitis were included.
The nasal polyps and mucosal specimens of all patients were collected and analyzed by Western Blot.
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We investigated the expression of EGR2 in patients with nasal polyps through immunohistochemistry.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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expression of EGR2
Time Frame: one months
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expression of EGR2 were analyzed by immunohistochemistry and Western Blot
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one months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Yong Luo, Doctor, Zunyi Medical College
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)
January 30, 2023
Primary Completion (ACTUAL)
February 1, 2023
Study Completion (ANTICIPATED)
May 5, 2023
Study Registration Dates
First Submitted
February 7, 2023
First Submitted That Met QC Criteria
February 9, 2023
First Posted (ACTUAL)
February 13, 2023
Study Record Updates
Last Update Posted (ACTUAL)
February 13, 2023
Last Update Submitted That Met QC Criteria
February 9, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- [2018]1182
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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