Chronic Obstructive Pulmonary DiseaseEarly Phase 1NCT04069052
The Effect of Inhaled Nitric Oxide on Deadspace in COPD
A Early Phase 1 study testing Nitric Oxide in people with Chronic Obstructive Pulmonary Disease, run by Dr. Denis O'Donnell at 1 site in Canada.
Trial summary
Chronic obstructive pulmonary disease (COPD) is a progressive disease of the respiratory system that generally develops as a result of smoking. Most people with COPD are classified as having "mild" disease severity and may not have significantly impaired lung function (e.g. Read more about this study
- Who is it for?
- Ages 45 years and older
- Conditions the study is for
- Chronic Obstructive Pulmonary Disease
- What is being tested?
- Nitric Oxide
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 13 participants
- Where
- 1 siteCanada
- Study dates
- 1 Sep 2021to 30 May 2023
- Phase
- Early Phase 1
- 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 45 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- clinically stable as defined by stable hemodynamic status, optimized medical treatment, no changes in medication dosage or frequency of administration with no hospital admission in the preceeding 6 weeks
- current or ex-smokers (>=20 pack-years)
- male or female >45 years of age
- mild COPD as defined by Medical Research Council dyspnea scale >=3 and post-bronchodilator FEV1 >=80% predicted and FEV1/FVC <0.7 and <LLN
- ability to perform all study procedures and provide/sign informed consent
Who cannot join
- women of childbearing age who are pregnant or trying to become pregnant
- active cardiopulmonary disease or other comorbidities that could contribute to dyspnea and exercise limitation
- important contraindications to clinical exercise testing, including inability to exercise because of neuromuscular or musculoskeletal disease(s)
- use of daytime oxygen, or exercise-induced O2 desaturation to <80% on room air
- body mass index (BMI) <18.5 or =>35.0 kg/m2
- echocardiographic evidence of pulmonary hypertension
- prior history of pulmonary thromboembolism or systemic vasculopathy
Trial locations and contacts
1 site in 1 country.
Canada1 site
Respiratory Investigation Unit, Kingston General Hospital
Kingston, Ontario, K7L 2V7
About this study
Official title: The Effect of Inhaled Nitric Oxide (iNO) on Physiologic Dead Space in Patients With Mild Chronic Obstructive Pulmonary Disease
Chronic obstructive pulmonary disease (COPD) is a progressive disease of the respiratory system that generally develops as a result of smoking. Most people with COPD are classified as having "mild" disease severity and may not have significantly impaired lung function (e.g. flow) as measured by traditional lung function tests. However, multiple studies have shown that patients with mild disease already have significant damage to the small airways and blood vessels of the pulmonary system. This results in a considerable portion of the lung that does not participate in gas exchange, a phenomenon called physiologic dead space. Mild COPD patients develop symptoms of intolerable breathlessness early in exercise compared with healthy individuals. Previous studies have shown that pulmonary vasodilators, which locally increase blood vessel radius, may improve gas exchange and reduce symptoms of breathlessness in patients with mild COPD. Therefore, the objective of this study is to determine the effect of reducing dead space with a pulmonary vasodilator on the intensity of breathlessness during exercise in patients with mild COPD. This five visit, double-blinded, placebo-controlled crossover study will test the impact of inhaled nitric oxide, a direct vasodilator, during cardiopulmonary exercise on dead space and breathlessness intensity. Use of an esophageal catheter during testing will additionally permit measurement of neural drive to breathe and pulmonary mechanics throughout the protocol. Though patients with mild COPD represent the majority of the COPD population, their symptoms remain poorly managed by current, inefficient standard of care. The proposed study will examine dead space reduction as a novel therapeutic target for improving breathlessness and exercise tolerance in patients with mild COPD.
Read the detailed description
This study will recruit 20 current or ex-smokers who meet the criteria for mild chronic obstructive pulmonary disease (COPD), measured by lung function tests. Participation is voluntary and participants may withdraw from the study at any time.
Procedures:
General Medical Examination: All participants will undergo a physical examination conducted by a physician. Concomitant medications will be recorded as well as body height and weight; blood pressure; heart rate rhythm using a 12-lead electrocardiogram (ECG); and blood oxygen saturation. The physician will identify any contraindications to exercise testing that would prevent safe participation.
Pulmonary Function Tests: Standard lung function tests include: spirometry (measuring respiratory flow during a maximal breath outward); body plethysmography (measuring lung volumes); diffusing capacity for carbon monoxide (DLCO; measuring gas exchange across the lung); maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) maneuvers (evaluating respiratory muscle strength); and impulse oscillometry (IOS; measuring lung mechanics). Each test will be performed at least 2-3 times to ensure the results are consistent. For all tests, the participant will breathe through a rubber mouthpiece with nose clips on to occlude the nasal passage.
Cardiopulmonary Exercise Tests: The participants will perform exercise on a stationary bicycle at each visit. While exercising, they will breathe through a mouthpiece with nose clips on, which allows for the breath-by-breath recording of physiologic variables throughout exercise. For each test, the participant will begin by sitting on the bike at rest (no pedaling) for approximately 6 minutes to establish a consistent measure of their baseline breathing. They will then begin pedaling for 1 minute against no resistance to warm-up. The load will then increase either by 10 Watts every minute (Visit 1) or to a constant work rate that will be maintained for 4 minutes (Visits 2-5). Every 2 minutes, the participant will be asked to take a full breath all the way in (an inspiratory capacity (IC) maneuver). The participant will also be asked to rate their breathing discomfort, their leg discomfort, how unpleasant their breathing feels, and how difficult it is to breathe in and out, using a 10-point Borg Scale.
Diaphragm EMG and Respiratory Pressure Measurements: Before exercise, a topical anaesthetic spray will be applied to the nasal passages and throat and a thin catheter (diameter 2 mm) will be inserted by experienced personnel through the nose down the throat and into the esophagus ("food tube") and top part of stomach. This catheter measures the electric activity (EMG) of the diaphragm, which provides useful information about the inspiratory drive to breathe. It also measures pressures in the esophagus within the chest as well as in the stomach, which gives useful information about the work of breathing and breathing mechanics.
Blood Sampling: Small samples of blood will be taken from the earlobe before exercise, at 2-minute intervals during exercise, and after exercise. The participant's earlobe will be warmed using a warm, damp cloth (ensuring adequate blood flow to the skin surface) throughout the baseline rest period and exercise. A very small puncture will be made using a lancet (similar to a very fine needle-tip), and blood will be collected in small glass tubes < 1mm in size. These samples will be analysed for their blood gas content (oxygen and carbon dioxide), variables needed to calculate dead space (the proportion of the lung unable to adequately participate in gas exchange).
Study design: This will be a single-centre, randomized, double-blind, placebo-controlled crossover study evaluating the effects of inhaled nitric oxide on the intensity of breathlessness and the physiological responses to a standardized exercise task. After giving written informed consent, participants will complete 5 visits, each conducted in the morning 2-7 days apart.
Visit 1 (Screening): The participants will have a detailed medical history taken and physical examination conducted by a study physician. The participants will also have their symptoms of COPD evaluated by standard written questionnaires [modified Medical Research Council (mMRC) dyspnea scale, Baseline Dyspnea Index (BDI), and COPD Assessment Test (CAT)]. These questionnaires will be explained to the participant by the study personnel and will be used to determine if the participants meet the criteria of having moderate-to-severe activity-related breathlessness. The participants will then undergo a series of pulmonary (lung) function tests at rest to determine lung function. Participants will complete a symptom-limited, incremental workload, cardiopulmonary exercise test on a stationary bicycle to determine their maximal work rate (Wmax). The participant will exercise on the bike for as long as they can, with the resistance increasing by 10 Watts every 1 min (see description above). Cardiac status will be monitored by 12-lead ECG. Heart rate, oxygen saturation (SpO2), and blood pressure will be monitored throughout exercise.
Visits 2 \& 3 (Run-In): The participants will be familiarized with the 4-min standardized cycle exercise test and breathing apparatus that will be completed for the remaining visits. This cycle exercise test will be performed at a constant load. The initial resistance selected will be 75% of their maximum workload (Wmax; determined from exercise test in Visit 1) with adjustments to the load made as needed. The goal of the resulting 4-min exercise test is to have a standardized protocol that allows the participants to become sufficiently breathless to assess the potential therapeutic effect of nitric oxide while not being so intense as to prevent them from completing the test.
Visits 4 and 5 (Treatment): The participants will complete the 4-min cycle exercise test at the work rate established in Visits 2 and 3 while breathing from a gas mixture consisting of either 1) inhaled nitric oxide (800 ppm) or 2) placebo (room air), each on a background of room air (21% oxygen; remainder nitrogen). Tests at Visits 4 and 5 will include detailed measurements of diaphragm electric activity (EMG) and respiratory mechanical measurements. Blood samples will be collected as described above: before exercise, at 2-minute intervals throughout exercise, and at the end of exercise.
- Conditions
- Chronic Obstructive Pulmonary Disease
- Being tested
- Nitric Oxide, Placebo
- Keywords
- Dyspnea, Exertional Dyspnea, Dead Space, Exercise, Inspiratory Neural Drive
- Medical subject headings
- Pulmonary Disease, Chronic Obstructive, Dyspnea, Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Nitric OxideDrug
Also called SoKinox
Gaseous pulmonary vasodilator, SoKinox (nitric oxide) flowed into a mask and breathed in.
PlaceboDrug
Also called Room air
Room air (placebo) flowed into a mask and breathed in.
| Study group | Role | What they receive |
|---|---|---|
| Inhaled Nitric Oxide | Experimental | Inhaled nitric oxide administered throughout 4 min exercise protocol at 800 ppm. Receives: Drug: Nitric Oxide |
| Placebo | Placebo comparator | Inhaled room air administered throughout 4 min exercise protocol at FiO2 = 0.21. Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Dyspnea Intensity
Primary objective is to measure perceptual (e.g. intensity of dyspnea and leg discomfort) responses at isotime (maximum exercise time achieved by all participants) during a standardized cardiopulmonary exercise testing (cycle ergometer).
Measured: At 4 minutes from start of exercise
Inspiratory neural drive
Primary objective is to measure inspiratory neural drive (IND) by diaphragm activation (EMGdi/EMGdi max) at isotime (maximum exercise time achieved by all participants) during cardiopulmonary exercise testing (cycle ergometer).
Measured: At 4 minutes from start of exercise
Secondary outcomes (5)
Lung volumes
Secondary objective is to measure lung volumes at isotime (maximum exercise time achieved by all participants) during cardiopulmonary exercise testing (cycle ergometer).
Measured: At 4 minutes from start of exercise
Trans-diaphragmatic Pressure (Pdi)
Secondary objective is to measure trans-diaphragmatic pressure (Pdi) at isotime (maximum exercise time achieved by all participants) during cardiopulmonary exercise testing (cycle ergometer).
Measured: At 4 minutes from start of exercise
Gastric Pressure (Pga)
Secondary objective is to measure gastric pressure (Pga) at isotime (maximum exercise time achieved by all participants) during cardiopulmonary exercise testing (cycle ergometer).
Measured: At 4 minutes from start of exercise
Esophageal Pressure (Pes)
Secondary objective is to measure esophageal pressure (Pes) at isotime (maximum exercise time achieved by all participants) during cardiopulmonary exercise testing (cycle ergometer).
Measured: At 4 minutes from start of exercise
Metabolic and gas exchange
Secondary objective is to measure metabolic and gas exchage (earlobe blood samples analyzed for blood gas content) at isotime (maximum exercise time achieved by all participants) during cardiopulmonary exercise testing (cycle ergometer).
Measured: At 4 minutes from start of exercise
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Aug 2019
- Study start1 Sep 2021
- Primary completion30 May 2023
- Study completion30 May 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Obstructive Pulmonary DiseaseStudies 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
- Early Phase 1
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Model description
- Single-centre, double-blinded, crossover study
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 13 participants (actual)
Sponsor and investigators
- Lead sponsor
- Dr. Denis O'Donnell
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Dr. Denis O'Donnell, Queen's University
- Investigators
- Denis E O'Donnell, MD, Principal investigator, Queen's University, Respiratory Investigation Unit
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04069052
- Sponsor's protocol ID
- DMED-2274-19
- Status last verified
- Apr 2024
- First submitted
- 11 Jul 2019
- Last updated
- 3 Apr 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 3 Apr 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Inhaled Nitric Oxide (iNO) on Physiologic Dead Space in Patients With Mild Chronic Obstructive Pulmonary Disease
- ClinicalTrials.gov ID
- NCT04069052
- Acronym / sponsor ID
- DMED-2274-19
- Conditions
- Chronic Obstructive Pulmonary Disease
- Keywords
- Dyspnea, Exertional Dyspnea, Dead Space, Exercise, Inspiratory Neural Drive
- Phase
- Early Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 13 participants (actual)
- Lead sponsor
- Dr. Denis O'DonnellUniversity, hospital or other
- Study start
- 1 Sep 2021 (actual)
- Primary completion
- 30 May 2023 (actual)
- Study completion
- 30 May 2023 (actual)
- First posted
- 28 Aug 2019 (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.
Chronic obstructive pulmonary disease (COPD) is a progressive disease of the respiratory system that generally develops as a result of smoking. Most people with COPD are classified as having "mild" disease severity and may not have significantly impaired lung function (e.g. flow) as measured by traditional lung function tests. However, multiple studies have shown that patients with mild disease already have significant damage to the small airways and blood vessels of the pulmonary system. This results in a considerable portion of the lung that does not participate in gas exchange, a phenomenon called physiologic dead space. Mild COPD patients develop symptoms of intolerable breathlessness early in exercise compared with healthy individuals. Previous studies have shown that pulmonary vasodilators, which locally increase blood vessel radius, may improve gas exchange and reduce symptoms of breathlessness in patients with mild COPD. Therefore, the objective of this study is to determine the effect of reducing dead space with a pulmonary vasodilator on the intensity of breathlessness during exercise in patients with mild COPD. This five visit, double-blinded, placebo-controlled crossover study will test the impact of inhaled nitric oxide, a direct vasodilator, during cardiopulmonary exercise on dead space and breathlessness intensity. Use of an esophageal catheter during testing will additionally permit measurement of neural drive to breathe and pulmonary mechanics throughout the protocol. Though patients with mild COPD represent the majority of the COPD population, their symptoms remain poorly managed by current, inefficient standard of care. The proposed study will examine dead space reduction as a novel therapeutic target for improving breathlessness and exercise tolerance in patients with mild COPD.
Detailed description
This study will recruit 20 current or ex-smokers who meet the criteria for mild chronic obstructive pulmonary disease (COPD), measured by lung function tests. Participation is voluntary and participants may withdraw from the study at any time.
Procedures:
General Medical Examination: All participants will undergo a physical examination conducted by a physician. Concomitant medications will be recorded as well as body height and weight; blood pressure; heart rate rhythm using a 12-lead electrocardiogram (ECG); and blood oxygen saturation. The physician will identify any contraindications to exercise testing that would prevent safe participation.
Pulmonary Function Tests: Standard lung function tests include: spirometry (measuring respiratory flow during a maximal breath outward); body plethysmography (measuring lung volumes); diffusing capacity for carbon monoxide (DLCO; measuring gas exchange across the lung); maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) maneuvers (evaluating respiratory muscle strength); and impulse oscillometry (IOS; measuring lung mechanics). Each test will be performed at least 2-3 times to ensure the results are consistent. For all tests, the participant will breathe through a rubber mouthpiece with nose clips on to occlude the nasal passage.
Cardiopulmonary Exercise Tests: The participants will perform exercise on a stationary bicycle at each visit. While exercising, they will breathe through a mouthpiece with nose clips on, which allows for the breath-by-breath recording of physiologic variables throughout exercise. For each test, the participant will begin by sitting on the bike at rest (no pedaling) for approximately 6 minutes to establish a consistent measure of their baseline breathing. They will then begin pedaling for 1 minute against no resistance to warm-up. The load will then increase either by 10 Watts every minute (Visit 1) or to a constant work rate that will be maintained for 4 minutes (Visits 2-5). Every 2 minutes, the participant will be asked to take a full breath all the way in (an inspiratory capacity (IC) maneuver). The participant will also be asked to rate their breathing discomfort, their leg discomfort, how unpleasant their breathing feels, and how difficult it is to breathe in and out, using a 10-point Borg Scale.
Diaphragm EMG and Respiratory Pressure Measurements: Before exercise, a topical anaesthetic spray will be applied to the nasal passages and throat and a thin catheter (diameter 2 mm) will be inserted by experienced personnel through the nose down the throat and into the esophagus ("food tube") and top part of stomach. This catheter measures the electric activity (EMG) of the diaphragm, which provides useful information about the inspiratory drive to breathe. It also measures pressures in the esophagus within the chest as well as in the stomach, which gives useful information about the work of breathing and breathing mechanics.
Blood Sampling: Small samples of blood will be taken from the earlobe before exercise, at 2-minute intervals during exercise, and after exercise. The participant's earlobe will be warmed using a warm, damp cloth (ensuring adequate blood flow to the skin surface) throughout the baseline rest period and exercise. A very small puncture will be made using a lancet (similar to a very fine needle-tip), and blood will be collected in small glass tubes < 1mm in size. These samples will be analysed for their blood gas content (oxygen and carbon dioxide), variables needed to calculate dead space (the proportion of the lung unable to adequately participate in gas exchange).
Study design: This will be a single-centre, randomized, double-blind, placebo-controlled crossover study evaluating the effects of inhaled nitric oxide on the intensity of breathlessness and the physiological responses to a standardized exercise task. After giving written informed consent, participants will complete 5 visits, each conducted in the morning 2-7 days apart.
Visit 1 (Screening): The participants will have a detailed medical history taken and physical examination conducted by a study physician. The participants will also have their symptoms of COPD evaluated by standard written questionnaires [modified Medical Research Council (mMRC) dyspnea scale, Baseline Dyspnea Index (BDI), and COPD Assessment Test (CAT)]. These questionnaires will be explained to the participant by the study personnel and will be used to determine if the participants meet the criteria of having moderate-to-severe activity-related breathlessness. The participants will then undergo a series of pulmonary (lung) function tests at rest to determine lung function. Participants will complete a symptom-limited, incremental workload, cardiopulmonary exercise test on a stationary bicycle to determine their maximal work rate (Wmax). The participant will exercise on the bike for as long as they can, with the resistance increasing by 10 Watts every 1 min (see description above). Cardiac status will be monitored by 12-lead ECG. Heart rate, oxygen saturation (SpO2), and blood pressure will be monitored throughout exercise.
Visits 2 \& 3 (Run-In): The participants will be familiarized with the 4-min standardized cycle exercise test and breathing apparatus that will be completed for the remaining visits. This cycle exercise test will be performed at a constant load. The initial resistance selected will be 75% of their maximum workload (Wmax; determined from exercise test in Visit 1) with adjustments to the load made as needed. The goal of the resulting 4-min exercise test is to have a standardized protocol that allows the participants to become sufficiently breathless to assess the potential therapeutic effect of nitric oxide while not being so intense as to prevent them from completing the test.
Visits 4 and 5 (Treatment): The participants will complete the 4-min cycle exercise test at the work rate established in Visits 2 and 3 while breathing from a gas mixture consisting of either 1) inhaled nitric oxide (800 ppm) or 2) placebo (room air), each on a background of room air (21% oxygen; remainder nitrogen). Tests at Visits 4 and 5 will include detailed measurements of diaphragm electric activity (EMG) and respiratory mechanical measurements. Blood samples will be collected as described above: before exercise, at 2-minute intervals throughout exercise, and at the end of exercise.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 2
- Model description
- Single-centre, double-blinded, crossover study
| Arm | Type | Receives |
|---|---|---|
| Inhaled Nitric Oxide | Experimental | Drug: Nitric OxideInhaled nitric oxide administered throughout 4 min exercise protocol at 800 ppm. |
| Placebo | Placebo comparator | Drug: PlaceboInhaled room air administered throughout 4 min exercise protocol at FiO2 = 0.21. |
Who may qualify
- Ages
- 45 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- clinically stable as defined by stable hemodynamic status, optimized medical treatment, no changes in medication dosage or frequency of administration with no hospital admission in the preceeding 6 weeks
- current or ex-smokers (>=20 pack-years)
- male or female >45 years of age
- mild COPD as defined by Medical Research Council dyspnea scale >=3 and post-bronchodilator FEV1 >=80% predicted and FEV1/FVC <0.7 and <LLN
- ability to perform all study procedures and provide/sign informed consent
Key exclusion criteria (7 listed)
- women of childbearing age who are pregnant or trying to become pregnant
- active cardiopulmonary disease or other comorbidities that could contribute to dyspnea and exercise limitation
- important contraindications to clinical exercise testing, including inability to exercise because of neuromuscular or musculoskeletal disease(s)
- use of daytime oxygen, or exercise-induced O2 desaturation to <80% on room air
- body mass index (BMI) <18.5 or =>35.0 kg/m2
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 |
|---|---|---|
| Nitric OxideAlso: SoKinoxGaseous pulmonary vasodilator, SoKinox (nitric oxide) flowed into a mask and breathed in. | Drug | Inhaled Nitric Oxide |
| PlaceboAlso: Room airRoom air (placebo) flowed into a mask and breathed in. | Drug | Placebo |
Primary outcome
Dyspnea Intensity
Time frame: At 4 minutes from start of exercise
Primary objective is to measure perceptual (e.g. intensity of dyspnea and leg discomfort) responses at isotime (maximum exercise time achieved by all participants) during a standardized cardiopulmonary exercise testing (cycle ergometer).
Inspiratory neural drive
Time frame: At 4 minutes from start of exercise
Primary objective is to measure inspiratory neural drive (IND) by diaphragm activation (EMGdi/EMGdi max) at isotime (maximum exercise time achieved by all participants) during cardiopulmonary exercise testing (cycle ergometer).
5 secondary outcomes
Lung volumes
Time frame: At 4 minutes from start of exercise
Trans-diaphragmatic Pressure (Pdi)
Time frame: At 4 minutes from start of exercise
Gastric Pressure (Pga)
Time frame: At 4 minutes from start of exercise
Esophageal Pressure (Pes)
Time frame: At 4 minutes from start of exercise
Metabolic and gas exchange
Time frame: At 4 minutes from start of exercise
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Apr 2024.
- 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.
Denis E O'Donnell, MD principal investigator
Queen's University, Respiratory Investigation Unit
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Early Phase 1 study testing Nitric Oxide in people with Chronic Obstructive Pulmonary Disease, run by Dr. Denis O'Donnell at 1 site in Canada.
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 5 inclusion and 7 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: finished, as of the sponsor's last update on 3 Apr 2024. 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 Canada. 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 phase mean?
Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.
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 is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Dyspnea Intensity (time frame: At 4 minutes from start of exercise). 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?
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 3 Apr 2024.