Allergic RhinitisPhase 2/3NCT04790487
Chlorpheniramine Maleate Nasal Spray for Chronic Rhinitis
A Phase 2/3 study testing CPM in people with Allergic Rhinitis and Nasal Congestion, run by Larkin Community Hospital at 1 site in United States.
Trial summary
Allergic rhinitis is defined as the symptoms of sneezing, nasal itching, airflow obstruction, and, mostly, clear nasal discharge caused by IgE-mediated reactions against inhaled allergens and involving mucosal inflammation driven by T cells (Th2) auxiliary type 2. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Allergic Rhinitis, Nasal Congestion
- What is being tested?
- CPM
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 0 participants
- Where
- 1 siteUnited States
- Study dates
- 30 Jul 2019to 30 Dec 2021
- Phase
- Phase 2/3
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- No oral steroids
- No oral antihistamine
- No Nafasoline If the patient needs rescue treatment, he will go to the intervention arm with chlorpheniramine or with the combination of chlorpheniramine and fluticasone. If a participant experienced a severe acute nasal block, the investigator could authorize the use of a short course of oxymetazoline spray for a maximum of 3 days and a maximum total of 1 day during the treatment period. Oxymetazoline should not be used within 24 hours of a scheduled visit during the study.
Who cannot join
- Large (grade 3) polyps, indicating severe nasal obstruction
- Surgical treatment for nasal polyps during the last 3 months
- Cystic fibrosis
- Purulent nasal infection
- Allergic rhinitis
- Any disease likely to interfere with the study parameters or which gave evidence of any serious or unstable concurrent disease or psychological disorder
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Randomized Placebo Control Trial to Evaluate the Efficacy of Chlorpheniramine Maleate Nasal Spray vs. Placebo for Acute or Chronic Rhinitis
Allergic rhinitis is defined as the symptoms of sneezing, nasal itching, airflow obstruction, and, mostly, clear nasal discharge caused by IgE-mediated reactions against inhaled allergens and involving mucosal inflammation driven by T cells (Th2) auxiliary type 2. pollens and molds, as well as allergens from perennial interiors, such as dust mites, pets, pests, and some molds. The pattern of dominant allergens depends on the geographic region and degree of urbanization, but the general prevalence of sensitization to allergens does not vary among census districts in the United States. This research proposes to study a separate antihistamine in a nasal spray. It is important to note that this antihistamine is available without prescription (OTC) and has been studied intranasal since the 1950s1
Read the detailed description
Allergic rhinitis is defined as the symptoms of sneezing, nasal itching, airflow obstruction and, mostly, clear nasal discharge caused by IgE-mediated reactions against inhaled allergens and involving mucosal inflammation driven by T cells (Th2) auxiliary type 2. pollens and molds, as well as allergens from perennial interiors, such as dust mites, pets, pests and some molds. The pattern of dominant allergens depends on the geographic region and degree of urbanization, but the general prevalence of sensitization to allergens does not vary among census districts in the United States.2 Sensitization to inhaled allergens begins during the first year of life; Sensitization to indoor allergens precedes sensitization to pollens. Because viral respiratory infections occur frequently in young children and produce similar symptoms, it is very difficult to diagnose allergic rhinitis in the first 2 or 3 years of life. The prevalence of allergic rhinitis reaches its peak in the second to fourth decades of life and then gradually decreases.
The frequency of sensitization to inhaled allergens is increasing and is now more than 40% in many populations in the United States and Europe. The prevalence of allergic rhinitis in the United States is approximately 30%. Allergic rhinitis contributes to lost or unproductive time at work and school, to sleep problems and among affected children, to less participation in outdoor activities. In addition, children with allergic rhinitis are more likely than unaffected children to have myringotomy tubes placed and their tonsils and adenoids removed. The ability to control asthma in people with asthma and allergic rhinitis has been linked to the control of allergic rhinitis.
Most people with asthma have rhinitis. The presence of allergic rhinitis (seasonal or perennial) significantly increases the likelihood of asthma: up to 40% of people with allergic rhinitis have or will have asthma. It is also important to define the physiological functional breathing of obstructive sleep apnea (OSA). Functional or physiological breathing is through the nose, while OSA is the collapse of the muscles of the oropharyngeal airways. Nasal obstruction and OSA are usually comorbid. Therapies to increase nasal volume and airflow in compromised patients have a significant benefit in reducing the symptoms of nighttime and daytime respiratory disorders.
The nose represents more than 50% of the total resistance of the upper airway and plays an important role in the establishment of physiological functions such as humidification, heating and air filtration. The nasal mucosa is a dynamic organ controlled by the autonomic nervous system. Periodic nasal congestion and decongestion have been termed the "nasal cycle." In patients with permanent unilateral nasal obstruction, the nasal cycle can contribute to a significant increase in total resistance of the respiratory tract.
Each nasal inhalation mixes nitric oxide (NO) gas from the maxillary sinuses and is transported to the lungs. It is NOT necessary for the movement of the cilia in the paranasal sinuses to carry out the waste, it is anti-fungal, antibacterial and anti-viral, it is also important in the peripheral vasodilatation of the blood vessels. In selected patients, it was recommended that the final point to treat OSA be the restoration of nasal breathing. Resistance of the upper respiratory tract can cause an increase in blood pressure. Mouth breathing does not have any of the mechanisms of physiological protection, so that people with this condition are more prone to respiratory infections, as well as to dental sequelae (gum disease, open anterior bite). That is why the investigators propose to study the combination of an antihistamine with more than 60 years in the market that was studied intranasal in the 50s. Nowadays it is known that the combination of antihistamine have better effect, less side effects than oral treatments. In the US and Europe, a combination of steroids with antihistamine of European origin is available only by recipes and is highly expensive. This research proposes to study a separate antihistamine in a nasal spray. It is important to note that this antihistamine is available without prescription (OTC) and has been studied intranasal since the 1950s1,2.
Method
A multicenter, randomized, double-blind, 14-day study will be conducted during the spring of 2019. After starting 5 days of placebo therapy, 100 patients from each group with moderate to severe nasal symptoms will be randomized to treatment. with (1) chlorpheniramine nasal spray vs placebo (nasal saline). All treatments will be administered in the form of 1 spray per nostril twice a day. The main variable of effectiveness will be the change from the beginning in the total score of nasal symptoms (TNSS), which consists of nasal congestion, nasal discharge, nasal itching and sneezing. The main efficacy variables will be (1) the change from the beginning to day 14 in the total reflective nasal symptom score (TNSS) in the first 12 hours, which combines scores for rhinorrhea, sneezing, itchy nose and nasal congestion, and (2) Start of Action, based on the instant TNSS for 4 hours after the first dose of the study drug. During the double-blind treatment period, patients will record their symptom scores on daily cards twice a day (morning and afternoon). Patients older than or equal to 18 years will complete the questionnaire on the quality of life of rhinoconjunctivitis (RQLQ) at the beginning of the study and on day 14. Patients will be instructed to call the office at any time for any questions . Follow-up appointments will be in 1 week, two, and four weeks.
- Conditions
- Allergic Rhinitis, Nasal Congestion
- Being tested
- CPM, Placebo
- Keywords
- Nasal Spray, Chlorpheniramine
- Medical subject headings
- Rhinitis, Allergic, Nasal Obstruction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
CPMDrug
Also called Chlorpheniramine
one spray dose (~100 µL of the solution containing 1.25 mg CPM) per nostril twice a day
PlaceboDrug
Also called PLB
Saline
| Study group | Role | What they receive |
|---|---|---|
| Chlorpheniramine | Experimental | Chlorpheniramine (CPM) Receives: Drug: CPM |
| Control | Placebo comparator | Saline Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Daily Symptom Score (DSS)
Allergy daily symptoms score The daily symptom score (DSS) consists of six individual symptom scores: four nasal symptoms (runny nose, blocked nose, sneezing, and itchy nose) and two ocular symptoms (gritty feeling or red or itchy eyes, and watery eyes). 0 to 3: 0 = no symptoms; 1 = mild symptoms; 2 = moderate symptoms; and 3 = severe symptoms for a max of 18
Measured: 30 days
Visual Analogue Scale (VAS)
visual analogue scale is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured. The scale goes from 0 (no symptoms) to 10 (most severe)
Measured: 30 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Mar 2021
- Study start30 Jul 2019
- Primary completion30 Dec 2020
- Study completion30 Dec 2021
Why it stopped: Study Period Ended/Not Completed
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Allergic RhinitisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2/3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Two groups placebo control
- Masking
- Double blind
- Who is masked
- Participant, Care provider
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Larkin Community Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Marcos A Sanchez-Gonzalez, Principal investigator, Larkin Health System
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04790487
- Sponsor's protocol ID
- LCH-6-072019
- Status last verified
- Oct 2023
- First submitted
- 6 Mar 2021
- Last updated
- 16 Oct 2023
- Results posted
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Van Toor BS, Buchwald A, Stengele E, Trenk D, Gercek C, de Mey CM. Systemic bioavailability of nasally applied chlorphenamine maleate (0.4% nasal spray) relative to tablets administered perorally. Int J Clin Pharmacol Ther. 2001 Apr;39(4):173-8. doi: 10.5414/cpp39173.
PubMed 11332874
Study at a glance
From the registry record, last updated by the sponsor on 16 Oct 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized Placebo Control Trial to Evaluate the Efficacy of Chlorpheniramine Maleate Nasal Spray vs. Placebo for Acute or Chronic Rhinitis
- ClinicalTrials.gov ID
- NCT04790487
- Acronym / sponsor ID
- LCH-6-072019
- Conditions
- Allergic Rhinitis, Nasal Congestion
- Keywords
- Nasal Spray, Chlorpheniramine
- Phase
- Phase 2/3
- Study type
- Interventional
- Recruitment status
- WithdrawnReason stopped: Study Period Ended/Not Completed
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Larkin Community HospitalUniversity, hospital or other
- Study start
- 30 Jul 2019 (actual)
- Primary completion
- 30 Dec 2020 (actual)
- Study completion
- 30 Dec 2021 (actual)
- First posted
- 10 Mar 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Allergic rhinitis is defined as the symptoms of sneezing, nasal itching, airflow obstruction, and, mostly, clear nasal discharge caused by IgE-mediated reactions against inhaled allergens and involving mucosal inflammation driven by T cells (Th2) auxiliary type 2. pollens and molds, as well as allergens from perennial interiors, such as dust mites, pets, pests, and some molds. The pattern of dominant allergens depends on the geographic region and degree of urbanization, but the general prevalence of sensitization to allergens does not vary among census districts in the United States. This research proposes to study a separate antihistamine in a nasal spray. It is important to note that this antihistamine is available without prescription (OTC) and has been studied intranasal since the 1950s1
Detailed description
Allergic rhinitis is defined as the symptoms of sneezing, nasal itching, airflow obstruction and, mostly, clear nasal discharge caused by IgE-mediated reactions against inhaled allergens and involving mucosal inflammation driven by T cells (Th2) auxiliary type 2. pollens and molds, as well as allergens from perennial interiors, such as dust mites, pets, pests and some molds. The pattern of dominant allergens depends on the geographic region and degree of urbanization, but the general prevalence of sensitization to allergens does not vary among census districts in the United States.2 Sensitization to inhaled allergens begins during the first year of life; Sensitization to indoor allergens precedes sensitization to pollens. Because viral respiratory infections occur frequently in young children and produce similar symptoms, it is very difficult to diagnose allergic rhinitis in the first 2 or 3 years of life. The prevalence of allergic rhinitis reaches its peak in the second to fourth decades of life and then gradually decreases.
The frequency of sensitization to inhaled allergens is increasing and is now more than 40% in many populations in the United States and Europe. The prevalence of allergic rhinitis in the United States is approximately 30%. Allergic rhinitis contributes to lost or unproductive time at work and school, to sleep problems and among affected children, to less participation in outdoor activities. In addition, children with allergic rhinitis are more likely than unaffected children to have myringotomy tubes placed and their tonsils and adenoids removed. The ability to control asthma in people with asthma and allergic rhinitis has been linked to the control of allergic rhinitis.
Most people with asthma have rhinitis. The presence of allergic rhinitis (seasonal or perennial) significantly increases the likelihood of asthma: up to 40% of people with allergic rhinitis have or will have asthma. It is also important to define the physiological functional breathing of obstructive sleep apnea (OSA). Functional or physiological breathing is through the nose, while OSA is the collapse of the muscles of the oropharyngeal airways. Nasal obstruction and OSA are usually comorbid. Therapies to increase nasal volume and airflow in compromised patients have a significant benefit in reducing the symptoms of nighttime and daytime respiratory disorders.
The nose represents more than 50% of the total resistance of the upper airway and plays an important role in the establishment of physiological functions such as humidification, heating and air filtration. The nasal mucosa is a dynamic organ controlled by the autonomic nervous system. Periodic nasal congestion and decongestion have been termed the "nasal cycle." In patients with permanent unilateral nasal obstruction, the nasal cycle can contribute to a significant increase in total resistance of the respiratory tract.
Each nasal inhalation mixes nitric oxide (NO) gas from the maxillary sinuses and is transported to the lungs. It is NOT necessary for the movement of the cilia in the paranasal sinuses to carry out the waste, it is anti-fungal, antibacterial and anti-viral, it is also important in the peripheral vasodilatation of the blood vessels. In selected patients, it was recommended that the final point to treat OSA be the restoration of nasal breathing. Resistance of the upper respiratory tract can cause an increase in blood pressure. Mouth breathing does not have any of the mechanisms of physiological protection, so that people with this condition are more prone to respiratory infections, as well as to dental sequelae (gum disease, open anterior bite). That is why the investigators propose to study the combination of an antihistamine with more than 60 years in the market that was studied intranasal in the 50s. Nowadays it is known that the combination of antihistamine have better effect, less side effects than oral treatments. In the US and Europe, a combination of steroids with antihistamine of European origin is available only by recipes and is highly expensive. This research proposes to study a separate antihistamine in a nasal spray. It is important to note that this antihistamine is available without prescription (OTC) and has been studied intranasal since the 1950s1,2.
Method
A multicenter, randomized, double-blind, 14-day study will be conducted during the spring of 2019. After starting 5 days of placebo therapy, 100 patients from each group with moderate to severe nasal symptoms will be randomized to treatment. with (1) chlorpheniramine nasal spray vs placebo (nasal saline). All treatments will be administered in the form of 1 spray per nostril twice a day. The main variable of effectiveness will be the change from the beginning in the total score of nasal symptoms (TNSS), which consists of nasal congestion, nasal discharge, nasal itching and sneezing. The main efficacy variables will be (1) the change from the beginning to day 14 in the total reflective nasal symptom score (TNSS) in the first 12 hours, which combines scores for rhinorrhea, sneezing, itchy nose and nasal congestion, and (2) Start of Action, based on the instant TNSS for 4 hours after the first dose of the study drug. During the double-blind treatment period, patients will record their symptom scores on daily cards twice a day (morning and afternoon). Patients older than or equal to 18 years will complete the questionnaire on the quality of life of rhinoconjunctivitis (RQLQ) at the beginning of the study and on day 14. Patients will be instructed to call the office at any time for any questions . Follow-up appointments will be in 1 week, two, and four weeks.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, care provider)
- Number of arms
- 2
- Model description
- Two groups placebo control
| Arm | Type | Receives |
|---|---|---|
| Chlorpheniramine | Experimental | Drug: CPMChlorpheniramine (CPM) |
| Control | Placebo comparator | Drug: PlaceboSaline |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- No oral steroids
- No oral antihistamine
- No Nafasoline If the patient needs rescue treatment, he will go to the intervention arm with chlorpheniramine or with the combination of chlorpheniramine and fluticasone. If a participant experienced a severe acute nasal block, the investigator could authorize the use of a short course of oxymetazoline spray for a maximum of 3 days and a maximum total of 1 day during the treatment period. Oxymetazoline should not be used within 24 hours of a scheduled visit during the study.
Key exclusion criteria (6 listed)
- Large (grade 3) polyps, indicating severe nasal obstruction
- Surgical treatment for nasal polyps during the last 3 months
- Cystic fibrosis
- Purulent nasal infection
- Allergic rhinitis
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| CPMAlso: Chlorpheniramineone spray dose (~100 µL of the solution containing 1.25 mg CPM) per nostril twice a day | Drug | Chlorpheniramine |
| PlaceboAlso: PLBSaline | Drug | Control |
Primary outcome
Daily Symptom Score (DSS)
Time frame: 30 days
Allergy daily symptoms score The daily symptom score (DSS) consists of six individual symptom scores: four nasal symptoms (runny nose, blocked nose, sneezing, and itchy nose) and two ocular symptoms (gritty feeling or red or itchy eyes, and watery eyes). 0 to 3: 0 = no symptoms; 1 = mild symptoms; 2 = moderate symptoms; and 3 = severe symptoms for a max of 18
Visual Analogue Scale (VAS)
Time frame: 30 days
visual analogue scale is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured. The scale goes from 0 (no symptoms) to 10 (most severe)
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Oct 2023.
- Background: PubMed 11332874Van Toor BS, Buchwald A, Stengele E, Trenk D, Gercek C, de Mey CM. Systemic bioavailability of nasally applied chlorphenamine maleate (0.4% nasal spray) relative to tablets administered perorally. Int J Clin Pharmacol Ther. 2001 Apr;39(4):173-8. doi: 10.5414/cpp39173.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Marcos A Sanchez-Gonzalez principal investigator
Larkin Health System
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2/3 study testing CPM in people with Allergic Rhinitis and Nasal Congestion, run by Larkin Community Hospital at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: withdrawn, as of the sponsor's last update on 16 Oct 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this combined phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was withdrawn before enrolling participants, so there are no results.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Daily Symptom Score (DSS) (time frame: 30 days). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04790487, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Oct 2023.