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Completed

NCT Number: NCT03226431

Use of ARINA-1 in an Intermediate Size Patient Population of Bilateral Lung Transplant Patients With CLAD Grade 0

To treat an intermediate size patient population of bilateral lung transplant patients with CLAD-0.

Completed

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Key information

Conditions

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Duke University Medical Center

Durham, North Carolina, 27710, United States

About this study

To treat an intermediate size patient population of bilateral lung transplant patients with CLAD-0. Treating physicians will follow standard of care for patients and monitor pulmonary function, fractional exhaled nitric oxide and quality of life of the patients.

Patient safety will be monitored by assessing changes in these parameters, as well as changes in standard of care measurements (e.g., laboratory values and x-ray images).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • >6 months post-bilateral lung transplant
  • Any patient with a stable FEV1 or a decline that is < 20% from baseline.
  • No current signs of infection
  • No current signs of rejection
  • >21 years old
  • Routinely followed at the enrolling site
  • Capable of giving informed consent

Exclusion criteria

  • Interstitial or peribronchial/peribronchiolar fibrosis on transbronchial biopsy
  • Evidence of active congestive heart failure or symptomatic coronary artery disease, in the opinion of the site investigator
  • CLAD grade 1 or higher
  • Currently on any ICS therapy
  • Initiation of chronic azithromycin within 1 month of study enrollment (chronic azithromycin use defined as azithromycin 250mg or 500mg daily or every Monday, Wednesday, Friday)
  • Positive pregnancy test at screening, if female and of child bearing potential

Treatment and study plan

ascorbic acid

Drug

ARINA-1 (inhaled ascorbic acid 88 mg/ml) will be nebulized twice daily for 3 months using a PARI eFlow nebulizer

Other names: ARINA-1

Primary outcomes

  1. Changes in FEV1

    Time frame: Baseline, 1 month, 3 months, 6 months, 12 months

    Each individual's changes in pulmonary function will be assessed using the linear slope of FEV1 change from enrollment to the end of the treatment period.

  2. Changes in FENO

    Time frame: Baseline

    Each individual's changes in FENO will be assessed using the change in mean baseline FENO measurements to the mean measurements post-ARINA-1 use.

  3. Changes in Quality of Life

    Time frame: Baseline, 12 months

    Patient-reported quality of life measures assessed pre- and post-ARINA-1 will be compared for each participant.

Sponsors and collaborators

Lead sponsor

Duke University

Other

Registry information

Official study title

Use of ARINA-1 in an Intermediate Size Patient Population of Bilateral Lung Transplant Patients With CLAD Grade 0 at Duke University to Improve FEV1

Acronym: ARINA-1

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Jul 21, 2017
Registry last updated
Jul 5, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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