AsthmaNCT02809235
Fatty Acids in Airway Smooth Muscle of Asthmatics
A study testing coconut oil in people with Asthma, run by Brigham and Women's Hospital at 1 site in United States.
Trial summary
In this proof of concept study, the investigators aim to determine if supplementation with coconut oil causes an increase in cholecystokinin and cholecystokinin receptor expression in the airway smooth muscle of lean asthmatics, and whether these changes correlate with changes in airway stiffness (estimated by… Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Asthma
- What is being tested?
- coconut oil
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 0 participants
- Where
- 1 siteUnited States
- Study dates
- Nov 2026to Nov 2029
- Phase
- Interventional
- 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 years and older
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Male and female participants, age 18 years and older at enrollment
- Never smokers or <10 pack year smoking history
- Body mass index (BMI) <25
- Clinical history consistent with asthma for >1 year
- No use of an inhaled corticosteroid in the prior 3mo
- Ability to perform reproducible spirometry according to ATS criteria
Show all 9Show fewer
- Baseline Forced expiratory volume in 1 second (FEV1) ≥ 60% predicted
- Presence of bronchodilator reversibility, as defined by a minimum of 12% and ≥ 200 ml improvement after 4 puffs of albuterol, each 90 μg
- Ability to provide informed consent, as evidenced by signing a copy of the consent form approved by the Institutional Review Board.
Who cannot join
- Supplementation with fatty acids within the last 3 months
- BMI ≥25
- Pregnant or nursing
- History of smoking (cigarettes, cigars, pipes, marijuana or any other substances) within the past 1 year, or >10 pack-years total
- Use of inhaled corticosteroid in the prior 3 mo
- Lack of bronchodilator response to 4 puffs of albuterol
Show all 9Show fewer
- Medical contraindication to bronchoscopy/biopsy, i.e inability to stop aspirin, anticoagulant, or antiplatelet at any point during the study; coagulopathy; inability to lay flat; asthma exacerbation requiring corticosteroids in the preceding 4 weeks; history of adverse reaction or allergy to sedatives; history of difficult airway, or past difficulty with intubation
- Major medical problems prohibiting study participation, i.e presence of chronic or active lung disease other than asthma or history of unstable significant medical illness other than asthma
- Evidence that the participant may be non-adherent to medication regimen, or may move from the performance site area before trial completion
Trial locations and contacts
1 site in 1 country.
United States1 site
Asthma Research Center, Brigham and Women's Hospital
Boston, Massachusetts, 02115
About this study
Official title: The Role of Cholecystokinin and the Cholecystokinin Receptor in the Airway Smooth Muscle of Asthmatics
In this proof of concept study, the investigators aim to determine if supplementation with coconut oil causes an increase in cholecystokinin and cholecystokinin receptor expression in the airway smooth muscle of lean asthmatics, and whether these changes correlate with changes in airway stiffness (estimated by bronchodilator reversibility, airway reactivity, and airway resistance) or symptom control.
The investigators propose a 5 week, single center trial in 20 lean patients with mild asthma (not taking inhaled corticosteroids) aged 18 and older. Subjects will supplement their usual diets with 3 tablespoons of coconut oil, a commercially available oil with high dodecanoic acid content, for 3 weeks. To quantify changes in airway smooth muscle cholecystokinin and cholecystokinin-receptor expression, each subject will undergo bronchoscopy with endobronchial biopsies before and after coconut oil ingestion.
Read more
For the secondary analysis, subjects will also complete spirometry with bronchodilator testing, methacholine challenge, body plethysmography, and an Asthma Control Questionnaire (ACQ) before and after the dietary intervention. This information will be used to compare the changes in airway smooth muscle cholecystokinin and cholecystokinin receptor expression to changes in bronchodilator reversibility, airway reactivity, airway resistance, and symptom control.
In the exploratory aims, the investigators will correlate the changes in airway smooth muscle cholecystokinin and cholecystokinin receptor expression with changes in FEV1 and peak flow measurements.
The investigators therefore hope to elucidate information about the mechanistic role of cholecystokinin in airway smooth muscle stiffness and contraction.
Read the detailed description
20 lean (BMI<25) nonsmokers at least 18 years of age with mild asthma will be recruited from the Asthma Research Center database. A sample size of 12 asthmatics is needed to have 80% power to detect a 3-fold increase in cholecystokinin (CCK) post dodecanoic acid ingestion at alpha level of 0.05, assuming the standard deviation is ≤2.25 in cycle scale. To account for probable incomplete retention, 20 subjects will be recruited. While the calculated standard deviation is 1.775, the investigators chose to base our calculations off of a larger standard deviation because of our small sample size.
Study subjects will be asked to come to 5 visits, described in detail below.
Visit 1: Eligibility Screen Pre-screened Volunteers will be asked not to take their short acting bronchodilators or ipratropium within 6 hours of this visit. They will complete a medical history that includes detailed information about past and current asthma medications, ACQ, physical exam with weight/BMI check and spirometry with bronchodilator testing. They will undergo body plethysmography to measure baseline airway resistance.
Visit 2: Eligibility Screen, methacholine challenge Subjects will return at any point during the 1-4 weeks allowed between visits 1 and 3. They will be told to not to take their short acting bronchodilators or ipratropium within 8 hours of this visit and to avoid caffeine (coffee, tea, cola drinks, and chocolate) the day of the visit. This visit will be short, comprised only of a methacholine challenge, to measure baseline airway reactivity.
Visit 3: Bronchoscopy Eligible subjects will be asked not to take aspirin, anticoagulant (e.g., warfarin) or antiplatelet (e.g., clopidogrel) medication in the 7 days prior to this second visit. They will also be told not to eat or drink within 6hrs of the visit.
At the beginning of the visit, subjects will be instructed on how to use a peak flow meter. Baseline peak flow measurements will be recorded. They will then undergo bronchoscopy with endobronchial biopsy. The investigators will perform laser capture on the biopsy samples to isolate the smooth muscle cells and quantify the cells' CCK and cholecystokinin receptor (CCK-AR) content via quantitative polymerase chain reaction (PCR).
The study participants will then be instructed to supplement their usual diets with 3 tablespoons of coconut oil (about 21.6g dodecanoic acid, 375 calories) daily for three weeks. The oil should be consumed uncooked so that its chemical form is unaltered. It can be swallowed by tablespoon or mixed into/spread on foods. The investigators recommend that it take the place of other fatty foods rather than be added to each subject's diet, so that subjects' overall daily caloric intake does not increase (and so that subjects do not gain weight).
The average adult ingests 0.8g of dodecanoic acid daily, according to a 2004 NHANES report. Dodecanoic acid is present at particularly high concentration in coconut oil (50% dodecanoic acid by weight). While the degree to which ingested dodecanoic acid reaches plasma and airway smooth muscle cells is unknown, prior trials confirm rise in plasma concentration of similar fatty acids (including gama linolenic acid, stearidonic acid, alpha linolenic acid, and eicosapentaenoic acid) after supplementation with as little as 0.25-4g daily for 3 weeks. The investigators have chosen to maximize the supplemented dose (to about 20g) so that any possible effect of dodecanoic acid on the airway smooth muscle is not missed. The 3 week duration is modeled after the aforementioned studies.
The investigators will provide each subject with a Drug Diary and peak flow meter. Subjects will be instructed to keep track of their daily coconut oil ingestion and peak flow measurements. They will be told to measure peak flow daily between 5 and 11 am, prior to the use of any morning inhalers, and to call the study coordinators if they experience a change in their asthma symptoms or if their measurements drop by more than 20% of their baseline. In addition, a study investigator will call each subject weekly to encourage compliance and to ensure that the subject has no questions or adverse events.
Visit 4: Followup exam, ACQ, pulmonary function tests After 3 weeks of coconut oil ingestion, subjects will return for a repeat physical exam with weight/BMI check and methacholine challenge. They will fill out a second ACQ and continue to supplement their diet with coconut oil until visit 5.
Visit 5: Followup pulmonary function tests, second bronchoscopy Subjects will return 1-3 days later for visit 5. They will again be told not to take aspirin, anticoagulant (e.g., warfarin) or antiplatelet (e.g., clopidogrel) medication in the 7 days prior to this final visit, and not to eat or drink within 6hrs of the visit.
The investigators will formally review each subject's Drug Diary and peak flow measurements. Eligible subjects will undergo spirometry, bronchodilator reversibility testing, body plethysmography, and bronchoscopy with endobronchial biopsy. The investigators will process the samples and compare the post-fatty acid ingestion outcomes to the baseline values.
- Conditions
- Asthma
- Being tested
- coconut oil
- Keywords
- asthma, smooth muscle, lauric acid, dietary supplement
- Medical subject headings
- Asthma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
coconut oilDietary supplement
3 tablespoons per day of supplemental coconut oil
| Study group | Role | What they receive |
|---|---|---|
| coconut oil | Experimental | Subjects will be instructed to supplement their diet with 3 tablespoons of coconut oil daily for three weeks. Receives: Dietary Supplement: coconut oil |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Airway Smooth Muscle (ASM) Cholecystokinin (CCK) and Cholecystokinin Receptor (CCK-AR) expression with coconut oil supplementation
Measured: 3 weeks
Secondary outcomes (4)
Change in ASM CCK and CCK-AR expression with coconut oil supplementation, versus change in bronchodilator reversibility.
Measured: 3 weeks
Change in ASM CCK and CCK-AR expression with coconut oil supplementation, versus change in bronchial hyperresponsiveness (PC20).
Measured: 3 weeks
Change in ASM CCK and CCK-AR expression with coconut oil supplementation, versus change in airway resistance
Measured: 3 weeks
Change in ASM CCK and CCK-AR expression with coconut oil supplementation, versus change in Asthma Control Questionnaire (ACQ) score.
Measured: 3 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Jun 2016 (estimated)
- Study startNov 2026 (estimated)
- Primary completionNov 2028 (estimated)
- Study completionNov 2029 (estimated)
Why it stopped: Study never started
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for AsthmaStudies of the same condition, open and under way.
- More trials run by Brigham and Women's HospitalThe sponsor's other registered studies.
- 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 N/A
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Brigham and Women's Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- Harvard School of Public Health (HSPH)
- Responsible party
- Principal investigator, Elliot Israel, MD, Brigham and Women's Hospital
- Investigators
- Elliot Israel, MD, Principal investigator, Asthma Research Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02809235
- Sponsor's protocol ID
- 2016P000273
- Status last verified
- Nov 2023
- First submitted
- 20 Jun 2016
- Last updated
- 23 Oct 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 23 Oct 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Role of Cholecystokinin and the Cholecystokinin Receptor in the Airway Smooth Muscle of Asthmatics
- ClinicalTrials.gov ID
- NCT02809235
- Acronym / sponsor ID
- 2016P000273
- Conditions
- Asthma
- Keywords
- asthma, smooth muscle, lauric acid, dietary supplement
- Study type
- Interventional
- Recruitment status
- WithdrawnReason stopped: Study never started
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Brigham and Women's HospitalUniversity, hospital or other
- Collaborators
- Harvard School of Public Health (HSPH)
- Study start
- Nov 2026 (estimated)
- Primary completion
- Nov 2028 (estimated)
- Study completion
- Nov 2029 (estimated)
- First posted
- 22 Jun 2016 (estimated)
- 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.
In this proof of concept study, the investigators aim to determine if supplementation with coconut oil causes an increase in cholecystokinin and cholecystokinin receptor expression in the airway smooth muscle of lean asthmatics, and whether these changes correlate with changes in airway stiffness (estimated by bronchodilator reversibility, airway reactivity, and airway resistance) or symptom control.
The investigators propose a 5 week, single center trial in 20 lean patients with mild asthma (not taking inhaled corticosteroids) aged 18 and older. Subjects will supplement their usual diets with 3 tablespoons of coconut oil, a commercially available oil with high dodecanoic acid content, for 3 weeks. To quantify changes in airway smooth muscle cholecystokinin and cholecystokinin-receptor expression, each subject will undergo bronchoscopy with endobronchial biopsies before and after coconut oil ingestion.
For the secondary analysis, subjects will also complete spirometry with bronchodilator testing, methacholine challenge, body plethysmography, and an Asthma Control Questionnaire (ACQ) before and after the dietary intervention. This information will be used to compare the changes in airway smooth muscle cholecystokinin and cholecystokinin receptor expression to changes in bronchodilator reversibility, airway reactivity, airway resistance, and symptom control.
In the exploratory aims, the investigators will correlate the changes in airway smooth muscle cholecystokinin and cholecystokinin receptor expression with changes in FEV1 and peak flow measurements.
The investigators therefore hope to elucidate information about the mechanistic role of cholecystokinin in airway smooth muscle stiffness and contraction.
Detailed description
20 lean (BMI<25) nonsmokers at least 18 years of age with mild asthma will be recruited from the Asthma Research Center database. A sample size of 12 asthmatics is needed to have 80% power to detect a 3-fold increase in cholecystokinin (CCK) post dodecanoic acid ingestion at alpha level of 0.05, assuming the standard deviation is ≤2.25 in cycle scale. To account for probable incomplete retention, 20 subjects will be recruited. While the calculated standard deviation is 1.775, the investigators chose to base our calculations off of a larger standard deviation because of our small sample size.
Study subjects will be asked to come to 5 visits, described in detail below.
Visit 1: Eligibility Screen Pre-screened Volunteers will be asked not to take their short acting bronchodilators or ipratropium within 6 hours of this visit. They will complete a medical history that includes detailed information about past and current asthma medications, ACQ, physical exam with weight/BMI check and spirometry with bronchodilator testing. They will undergo body plethysmography to measure baseline airway resistance.
Visit 2: Eligibility Screen, methacholine challenge Subjects will return at any point during the 1-4 weeks allowed between visits 1 and 3. They will be told to not to take their short acting bronchodilators or ipratropium within 8 hours of this visit and to avoid caffeine (coffee, tea, cola drinks, and chocolate) the day of the visit. This visit will be short, comprised only of a methacholine challenge, to measure baseline airway reactivity.
Visit 3: Bronchoscopy Eligible subjects will be asked not to take aspirin, anticoagulant (e.g., warfarin) or antiplatelet (e.g., clopidogrel) medication in the 7 days prior to this second visit. They will also be told not to eat or drink within 6hrs of the visit.
At the beginning of the visit, subjects will be instructed on how to use a peak flow meter. Baseline peak flow measurements will be recorded. They will then undergo bronchoscopy with endobronchial biopsy. The investigators will perform laser capture on the biopsy samples to isolate the smooth muscle cells and quantify the cells' CCK and cholecystokinin receptor (CCK-AR) content via quantitative polymerase chain reaction (PCR).
The study participants will then be instructed to supplement their usual diets with 3 tablespoons of coconut oil (about 21.6g dodecanoic acid, 375 calories) daily for three weeks. The oil should be consumed uncooked so that its chemical form is unaltered. It can be swallowed by tablespoon or mixed into/spread on foods. The investigators recommend that it take the place of other fatty foods rather than be added to each subject's diet, so that subjects' overall daily caloric intake does not increase (and so that subjects do not gain weight).
The average adult ingests 0.8g of dodecanoic acid daily, according to a 2004 NHANES report. Dodecanoic acid is present at particularly high concentration in coconut oil (50% dodecanoic acid by weight). While the degree to which ingested dodecanoic acid reaches plasma and airway smooth muscle cells is unknown, prior trials confirm rise in plasma concentration of similar fatty acids (including gama linolenic acid, stearidonic acid, alpha linolenic acid, and eicosapentaenoic acid) after supplementation with as little as 0.25-4g daily for 3 weeks. The investigators have chosen to maximize the supplemented dose (to about 20g) so that any possible effect of dodecanoic acid on the airway smooth muscle is not missed. The 3 week duration is modeled after the aforementioned studies.
The investigators will provide each subject with a Drug Diary and peak flow meter. Subjects will be instructed to keep track of their daily coconut oil ingestion and peak flow measurements. They will be told to measure peak flow daily between 5 and 11 am, prior to the use of any morning inhalers, and to call the study coordinators if they experience a change in their asthma symptoms or if their measurements drop by more than 20% of their baseline. In addition, a study investigator will call each subject weekly to encourage compliance and to ensure that the subject has no questions or adverse events.
Visit 4: Followup exam, ACQ, pulmonary function tests After 3 weeks of coconut oil ingestion, subjects will return for a repeat physical exam with weight/BMI check and methacholine challenge. They will fill out a second ACQ and continue to supplement their diet with coconut oil until visit 5.
Visit 5: Followup pulmonary function tests, second bronchoscopy Subjects will return 1-3 days later for visit 5. They will again be told not to take aspirin, anticoagulant (e.g., warfarin) or antiplatelet (e.g., clopidogrel) medication in the 7 days prior to this final visit, and not to eat or drink within 6hrs of the visit.
The investigators will formally review each subject's Drug Diary and peak flow measurements. Eligible subjects will undergo spirometry, bronchodilator reversibility testing, body plethysmography, and bronchoscopy with endobronchial biopsy. The investigators will process the samples and compare the post-fatty acid ingestion outcomes to the baseline values.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| coconut oil | Experimental | Dietary Supplement: coconut oilSubjects will be instructed to supplement their diet with 3 tablespoons of coconut oil daily for three weeks. |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (9 listed)
- Male and female participants, age 18 years and older at enrollment
- Never smokers or <10 pack year smoking history
- Body mass index (BMI) <25
- Clinical history consistent with asthma for >1 year
- No use of an inhaled corticosteroid in the prior 3mo
Key exclusion criteria (9 listed)
- Supplementation with fatty acids within the last 3 months
- BMI ≥25
- Pregnant or nursing
- History of smoking (cigarettes, cigars, pipes, marijuana or any other substances) within the past 1 year, or >10 pack-years total
- Use of inhaled corticosteroid in the prior 3 mo
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 |
|---|---|---|
| coconut oil3 tablespoons per day of supplemental coconut oil | Dietary supplement | coconut oil |
Primary outcome
Change in Airway Smooth Muscle (ASM) Cholecystokinin (CCK) and Cholecystokinin Receptor (CCK-AR) expression with coconut oil supplementation
Time frame: 3 weeks
4 secondary outcomes
Change in ASM CCK and CCK-AR expression with coconut oil supplementation, versus change in bronchodilator reversibility.
Time frame: 3 weeks
Change in ASM CCK and CCK-AR expression with coconut oil supplementation, versus change in bronchial hyperresponsiveness (PC20).
Time frame: 3 weeks
Change in ASM CCK and CCK-AR expression with coconut oil supplementation, versus change in airway resistance
Time frame: 3 weeks
Change in ASM CCK and CCK-AR expression with coconut oil supplementation, versus change in Asthma Control Questionnaire (ACQ) score.
Time frame: 3 weeks
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 23 Oct 2024.
- Individual participant dataSharing planned: Undecided
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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.
Elliot Israel, MD principal investigator
Asthma Research Center
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing coconut oil in people with Asthma, run by Brigham and Women's 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 9 inclusion and 9 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 23 Oct 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 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. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
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?
Change in Airway Smooth Muscle (ASM) Cholecystokinin (CCK) and Cholecystokinin Receptor (CCK-AR) expression with coconut oil supplementation (time frame: 3 weeks). 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 23 Oct 2024.