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NCT04878445Active, not recruiting

Tissue Engineering Approaches to Treat COPD

A Tissue Engineering Approach to Improve Lung Function and Clinical Outcome in Patients With COPD

Source: ClinicalTrials.gov · Last updated 4 Feb 2025

Brief summary (registry, in English)

The study is a pilot/laboratory study comparing lung tissue from control participants with tissue from COPD participants with a chronic bronchitis or emphysema phenotypes. Tissue will be characterised mechanically and biochemically. Lung cells, including DASCp63/Krt5 with a possible role in disease pathology, will be isolated, expanded in vitro, characterised, and banked. Biomaterials will be selected and tested with regards to mechanical and physical properties and selected for use in the production of TELEs with properties matched to healthy and diseased lung tissue. The resulting TELEs will be tested in an ex vivo tissue culture model to determine the extent of their integration with lung.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
30 Apr 2021
Start date
31 Aug 2017
Primary completion date
31 Dec 2024
Lead sponsor
University Hospitals of North Midlands NHS Trust
Diseases
Lung cancer
NCT number
NCT04878445

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 31 Aug 2017 to the primary completion date, 31 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Significant long term condition or lung pathology (infection, asthma, fibrotic lung diseases) other than that for which they have been referred for surgery.
    • Post Surgery

Lab values

  • Insufficient tissue removed to supply the laboratory study after consultation with the Consultant histopathologist.

Other

  • Patient unable to give informed consent

Who the study is looking for

  • Men or women aged over 18 years- .
  • Must be competent to give written informed consent.
  • Scheduled to undergo clinical indicated surgery to remove lung tissue.

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospitals of North Midlands NHS Trust
Coordinator of this site? Confirm its status
Stoke-on-TrentUnited KingdomUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.