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NCT01805713 · ClinicalTrials.gov registry record

Biomarkers of Injury and Destruction in the Cystic Fibrosis Lung

A clinical trial, sponsored by University of Minnesota.

Completed
Registry status
150
Enrollment target

NCT01805713: Completed study, sponsored by University of Minnesota.

NCT01805713 is a clinical trial that has completed, run by University of Minnesota. The registered enrollment target is 150 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01805713 has completed, sponsored by University of Minnesota.

COMPLETED
Registry status
150 participants
Enrollment target

Study Summary

Cystic fibrosis (CF) is the most common autosomal recessive genetic disease in Caucasians. It results in lung disease that affects quality of life and causes early death. Lung damage from CF starts in infancy and continues over time. Lung damage can negatively affect how the lung functions. It would be ideal to measure lung damage in CF patients in three instances: (1) During the first year of life after diagnosis by state newborn screening programs, (2) In children and adults over long periods of time (years), and (3) During times of illness (pulmonary exacerbation), to allow for better treatment and therapy to prevent loss of lung function. The lung is made of elastin, collagen and cartilage. When the lung is damaged by CF, these components break down into pieces that can be measured in urine, sputum and blood. These products may represent markers of lung injury. We believe that the levels of these markers will be increased over time in CF patients and even higher in patients who are sick with lung symptoms. The goal of my research is to measure the amount of lung breakdown products in urine, sputum and blood in infants, children and adults with CF during times when well and also during times of illness. I also hope to use new technologies involving the study of proteins and metabolites in samples like sputum, urine and blood to help provide new information regarding CF lung disease. These studies will help us to better treat CF lung disease.

Primary Outcome

Desmosine,Clara Cell Protein(CC10) and cathepsin B concentration in biological specimens.

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2012-12
Est. Completion 2017-12
University of Minnesota

966 total trials

What the finished NCT01805713 record still lists

NCT01805713 is an observational study that tracks outcomes without assigning an intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 0 interventions.

NCT01805713 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01805713 about?

NCT01805713 is a clinical study titled "Biomarkers of Injury and Destruction in the Cystic Fibrosis Lung". Cystic fibrosis (CF) is the most common autosomal recessive genetic disease in Caucasians. It results in lung disease that affects quality of life and causes early death. Lung damage from CF starts in infancy and continues over time. Lung damage can negatively affect how the lung functions. It would...

What is the current status of trial NCT01805713?

This trial is currently completed. The enrollment target is 150 participants. The study started on 2012-12. Estimated completion is 2017-12.

Who is sponsoring clinical trial NCT01805713?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT01805713, the US trial registry maintained by the National Library of Medicine. NCT01805713 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.