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Repeatability and Response Study of Absorptive Clearance Scans

T

Tim Corcoran

Status and phase

Completed
Phase 1

Conditions

Cystic Fibrosis

Treatments

Drug: inhaled hypertonic saline (7%)
Other: Absorptive clearance scan
Drug: mannitol inhalation powder

Study type

Interventional

Funder types

Other

Identifiers

NCT01887197
1RO1 HL108929-01 (B)

Details and patient eligibility

About

The investigators are developing a new nuclear medicine imaging technique for measuring liquid absorption in the airways that can be applied to screen new medications being developed to treat cystic fibrosis (CF). The investigators believe that the absorption of the small molecule radiopharmaceutical Indium 111 diethylene triamine pentaacetic acid (In-DTPA) will indicate changes in liquid absorption in the airways and demonstrate whether new CF medications will be effective. In this study the investigators will determine whether the imaging technique will demonstrate similar results when it is repeated on different days. They will also determine how their results change when subjects utilize several common CF medications.

Full description

Cystic Fibrosis (CF) is an autosomal recessive genetic disease, caused by mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) that impairs ion transport at epithelial surfaces. This results in the accumulation of dehydrated secretions in the airways and chronic infection and inflammation in the lungs, leading to significant morbidity and mortality. The investigators understanding of CF pathogenesis has increased substantially and many new targeted therapies are being developed to treat this disease, however, the measurements of clinical efficacy used to evaluate these therapies require long trials to demonstrate an effect. New translational techniques are needed to assess changes in the most basic aspects of the disease and allow for the rapid screening of disease-altering therapies. The investigators have recently developed a novel aerosol-based imaging technique to measure liquid absorption in the airways - a central pathophysiological process related to CFTR dysfunction. The investigators propose that airway liquid hyper-absorption is a key link between cellular defects in ion and fluid transport and progressive airway dysfunction in CF. Thus The investigators technique may provide a measure of disease severity and rapid indication of therapeutic correction in advance of currently available outcome measures.

Enrollment

24 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • subjects 18 years old or older with a diagnosis of cystic fibrosis as determined by sweat test or genotype and clinical symptoms who are clinically stable as determined by a physician co-investigator

Exclusion criteria

  • one second forced expiratory volume (FEV1) <50% of predicted
  • nursing mother
  • positive urine pregnancy test or unwilling to test
  • cigarette smoker
  • unwilling to stop hypertonic saline therapy for 72 hours prior to each test day
  • are intolerant to hypertonic saline (response only)
  • are intolerant to any inhaled therapies (response only)
  • fail mannitol tolerance testing (response only)
  • have a history of excessive (uncontrollable) coughing after an osmotic stimulus (response only)
  • have a history of hemoptysis (response only)

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

24 participants in 2 patient groups

Repeatability
Experimental group
Description:
Subjects perform two sequential absorptive clearance scans (within 30 days) to determine the repeatability of the technique. Subjects also perform a third scan two years later so that longitudinal change can be measured.
Treatment:
Other: Absorptive clearance scan
Response
Experimental group
Description:
Subjects perform three different absorptive clearance scans. One is a baseline measurement while the other two measure absorptive clearance after an intervention (inhaled hypertonic saline, mannitol inhalation powder).
Treatment:
Other: Absorptive clearance scan
Drug: mannitol inhalation powder
Drug: inhaled hypertonic saline (7%)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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