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Dietary Nitrate in COPD (CHB-BRJ-COPD)

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Nitrate rich beverage
Nitrate free beverage
Sponsored by
Royal College of Surgeons, Ireland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Obstructive Pulmonary Disease focused on measuring COPD, beetroot, dietary nitrate, nitric oxide

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Information consenting out-patients with a previous physician diagnosis of COPD
  • Clinically stable
  • Ambulatory

Exclusion Criteria:

  • Subjects who required supplemental oxygen for exercise
  • Subjects with pulmonary hypertension and angina
  • Intolerant to beetroot
  • Insulin dependent diabetes
  • Thyroid disease

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    Nitrate rich beverage

    Nitrate free beverage

    Arm Description

    Nitrate rich beverage will contain 140ml nitrate rich beetroot juice + 200ml blackcurrant juice containing 12.7mmol nitrate

    Nitrate free beverage will 140ml water + 200ml blackcurrant juice containing <0.5mmol nitrate

    Outcomes

    Primary Outcome Measures

    Change in Incremental Shuttle Walk Test Distance
    The change between day 1, time 0 and day 1, time 3h will be compared to the changes between day 8, time 0 and day 8, time 3h.

    Secondary Outcome Measures

    Full Information

    First Posted
    May 19, 2014
    Last Updated
    June 4, 2014
    Sponsor
    Royal College of Surgeons, Ireland
    Collaborators
    University College Dublin
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02148289
    Brief Title
    Dietary Nitrate in COPD
    Acronym
    CHB-BRJ-COPD
    Official Title
    Dietary Nitrate in COPD: A Double-blind, Randomized, Placebo-controlled, Crossover Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2014
    Overall Recruitment Status
    Completed
    Study Start Date
    November 2012 (undefined)
    Primary Completion Date
    March 2013 (Actual)
    Study Completion Date
    March 2013 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Royal College of Surgeons, Ireland
    Collaborators
    University College Dublin

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The acute consumption of dietary nitrate has been shown to improve exercise capacity in athletes, healthy adults and subjects with peripheral vascular disease. Many COPD patients have reduced exercise capacity, The investigators hypothesized that acute nitrate consumption, in the form of beetroot juice, might increase incremental shuttle walk test (ISWT) distance in COPD subjects.
    Detailed Description
    Acute consumption of dietary nitrate (as beetroot juice) has been shown to improve exercise capacity in athletes, healthy adults and subjects with peripheral vascular disease. Many COPD patients have reduced exercise capacity, The investigators hypothesized that acute nitrate consumption might increase incremental shuttle walk test (ISWT) distance in COPD subjects compared to a matched, low-nitrate drink. This study is a randomized, double-blind placebo-controlled, crossover trial. Resting blood pressure, phlebotomy and ISWT are performed. Following completion, each subject is randomized to consume beetroot juice or placebo. 3 hours later, the same assessments are repeated by the same people. After a 7d washout, the entire protocol is repeated with the crossover beverage.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Obstructive Pulmonary Disease
    Keywords
    COPD, beetroot, dietary nitrate, nitric oxide

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    ParticipantInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    12 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Nitrate rich beverage
    Arm Type
    Active Comparator
    Arm Description
    Nitrate rich beverage will contain 140ml nitrate rich beetroot juice + 200ml blackcurrant juice containing 12.7mmol nitrate
    Arm Title
    Nitrate free beverage
    Arm Type
    Placebo Comparator
    Arm Description
    Nitrate free beverage will 140ml water + 200ml blackcurrant juice containing <0.5mmol nitrate
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Nitrate rich beverage
    Other Intervention Name(s)
    Nitrate rich beetroot juice
    Intervention Description
    Following randomisation on day 1, subjects will consume either the nitrate or nitrate-free beverage and then the crossover beverage on day 8.
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Nitrate free beverage
    Other Intervention Name(s)
    Placebo beverage
    Intervention Description
    Following randomisation on day 1, subjects will consume either the nitrate or nitrate-free beverage and then the crossover beverage on day 8.
    Primary Outcome Measure Information:
    Title
    Change in Incremental Shuttle Walk Test Distance
    Description
    The change between day 1, time 0 and day 1, time 3h will be compared to the changes between day 8, time 0 and day 8, time 3h.
    Time Frame
    day 1, time 0, day 1, time 3h, day 8, time 0, day 8, time 3h
    Other Pre-specified Outcome Measures:
    Title
    Resting blood pressure
    Description
    The change between day 1, time 0 and day 1, time 3h will be compared to the changes between day 8, time 0 and day 8, time 3h.
    Time Frame
    day 1, time 0, day 1, time 3h, day 8, time 0, day 8, time 3h

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Information consenting out-patients with a previous physician diagnosis of COPD Clinically stable Ambulatory Exclusion Criteria: Subjects who required supplemental oxygen for exercise Subjects with pulmonary hypertension and angina Intolerant to beetroot Insulin dependent diabetes Thyroid disease
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Conor P Kerley, BSc
    Organizational Affiliation
    University College Dublin
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Liam J Cormican, MD
    Organizational Affiliation
    Royal College of Surgeons in Ireland
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Dietary Nitrate in COPD

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