Asthma L-Citrulline Pilot Study

NCT ID: NCT02943161

Last Updated: 2020-02-27

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 41 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-04-05
• Study Completion Date: 2019-03-31

Brief Summary

This study will evaluate whether treatment with L-citrulline, which is an amino acid found in some foods, can increase levels of L-arginine and thereby restore the concentration of nitric oxide (NO) in the airways.

Detailed Description

Research has shown that some obese asthmatics have a metabolic imbalance in which L-arginine levels are reduced. L-arginine is an amino acid that is used to make NO, a gas that is normally made in the bronchi and ensures that the lungs function properly. In this pilot study subjects with asthma that have an increased body mass index compatible with being obese, will be invited to participate in a short open-label treatment with 15g/day of L-citrulline for two weeks. Study participants will be asked to do lung function testing and donate blood before and after taking the supplement. L-citrulline is safe and well tolerated and has been used at much higher doses without significant side effects.

Conditions

Asthma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

L-Citrulline

In this pilot study subjects with asthma that have an increased body mass index compatible with being obese, will be invited to participate in a short open-label treatment with 15g/day of L-citrulline for two weeks. Study participants will be asked to do lung function testing and donate blood before and after taking the supplement. L-citrulline is safe and well tolerated and has been used at much higher doses without significant side effects.

Group Type: EXPERIMENTAL

L-Citrulline

Intervention Type: DIETARY_SUPPLEMENT

The purpose of this study is to see if citrulline supplementation will restore NO levels and lung function in subjects with asthma.

Interventions

L-Citrulline

The purpose of this study is to see if citrulline supplementation will restore NO levels and lung function in subjects with asthma.

Intervention Type: DIETARY_SUPPLEMENT

Eligibility Criteria

Inclusion Criteria

• Adequate completion of informed consent process with written documentation
• Male and female patients, 18 - 70 years old, inclusive
• Physician diagnosis of asthma (for medical records, ICD 10 coding for physician's diagnosis)
• All racial/ethnic backgrounds may participate
• BMI ≥ 30
• Treatment of controller asthma medication(s) ≥ 4 weeks
• Smoking history ≤10 pack years and no smoking in the last year
• V1 eNO ≤ 30ppb (may be repeated 3x during visit; lowest ppb will be kept)

Exclusion Criteria

• Respiratory tract infection within the 4 weeks prior to the study (may re-enroll after 4 weeks).
• Oral or systemic corticosteroid burst (for any indication) within the 4 weeks
• One-time doses, such as intra-articular injections into a shoulder or knee joint, require a 2-week washout.
• Asthma-related ER visit within the previous 4 weeks of Visit 1
• Significant concomitant medical illness, including (but not limited to)

• Heart disease
• Cancer
• Uncontrolled diabetes,
• Chronic renal failure (creatinine > 2.0) at Visit 1 (Associated with higher ADMA levels)
• Untreated sleep apnea
• Other chronic lung/respiratory diseases (COPD, IPF, etc.)
• High dose inhaled steroids (> 1000 mcg/day of Fluticasone or equivalent)
• Current statin use (statins lower ADMA levels); patients may stop statins with approval from their primary physician and enroll after a 6-week washout
• Positive urine pregnancy test at Visit 1 or at any time during the study
• Intolerance or allergy to L-arginine or L-citrulline
• Concomitant use of PDE5 drugs or oral mononitrates
• Participation in an intervention study, use of investigative drugs within the past 30 days or plans to enroll in such a trial during the study
• Unable or unlikely to complete study assessments in the opinion of the Investigator
• Study intervention poses undue risk to patient in the opinion of the Investigator
• Breastfeeding

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Colorado, Denver

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Fernando Holguin, MD, MPH

Role: PRINCIPAL_INVESTIGATOR

University of Colorado, Denver

Locations

University of Colorado

Aurora, Colorado, United States

Duke University

Durham, North Carolina, United States

Countries

United States

Other Identifiers

16-2041

Identifier Type: -

Identifier Source: org_study_id