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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00580892
Other study ID # 20064982
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date July 2007
Est. completion date July 2018

Study information

Verified date October 2022
Source University of California, Irvine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The researcher can use Optical coherence tomography a near-infrared diode to emit light that can produce images of the specimen under investigation and provide information about tissue abnormalities without causing damage.


Description:

The researcher can use Optical coherence tomography endoscopic imaging to improve diagnosis and treatment of airway and pleural malignancy. In the events of burn injury and smoke inhalation injury, the Optical coherence tomography can determine the change of the airway tissues and severity of airway injury. During endoscopic procedure the lesions will be biopsied and prepared by standard histologic methods. The Optical coherence tomography endoscopic imaging can measured histologic of the tissue samples and compared to standard histologic examination. The Optical coherence tomography endoscopic imaging can measured the epithelial thickness and compared to visual inspection of the mucosa on bronchoscopy.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 2018
Est. primary completion date July 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult 18 or older, male or female. - Plans for bronchoscopic with possible biopsy procedures. Exclusion Criteria: - Age less than 18 years of age - Not plan for bronchoscopic with possible biopsy procedures. - Pregnant or breastfeeding.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Optical Coherence Tomography imaging
Optical Coherence Tomography imaging

Locations

Country Name City State
United States Pulmonary and Critical Care Medicine Irvine California

Sponsors (2)

Lead Sponsor Collaborator
University of California, Irvine Beckman Laser Institute University of California Irvine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary histopathology up to 4 weeks
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