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NCT03485690Completed

Time-based Register and Analysis of COPD Endpoints

Source: ClinicalTrials.gov · Last updated 3 Sept 2026

Brief summary (registry, in English)

The Time-based Register and Analysis of COPD Endpoints (TRACE) study is prospective cohort study aiming at evaluating COPD patients using simple basic tools normally used in the clinic at hand of any physician. The objective of the study is to accomplish specific aims. 1) describing the disease variation over time. 2) defining different disease behaviours; and 3) evaluating the impact of different therapeutic approaches on this behaviour in the different patient types. TRACE is a single center non-interventional prospective observational cohort study of COPD patients. Upon identification of cases, patients are followed-up in yearly visits sine die until death or lost to follow-up. Starting in 2012, during the yearly visits clinical, functional, radiological and analytical information is recorded via a standardized questionnaire. Variables recorded were: socio-demographics, tobacco history, comorbidities, clinical presentation during the previous year, exacerbations and hospitalization in the previous year, current pharmacological and non-pharmacological treatments, and complementary tests, including at least chest radiology, pre- and post-bronchodilator spirometry, and analytical results. Endpoints include a variety of clinically relevant variables including disease phenotypic expression, diagnostic measures and therapeutic responses.

Status (registry)
Completed
Study type
Observational
Enrollment
1440 (actual)
First submitted
12 Feb 2018
Start date
1 Jan 2012
Primary completion date
15 Apr 2026
Lead sponsor
Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
Diseases
COPD
NCT number
NCT03485690

What you commit to

  • Study type: Observational
  • Participants enrolled: 1440
  • From 1 Jan 2012 to the primary completion date, 15 Apr 2026
  • 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

  • With other relevant comorbidity that conditions their respiratory care

Other

  • Do not sign informed consent.

Who the study is looking for

  • Adult patients
  • Diagnosed of COPD, according to the current recommendations
  • Evaluated in our COPD outpatient clinic in 2012 or the following years
  • With three years of follow-up at least

Age in the registry: 40 years to 90 years · Sex: All · Does not accept healthy volunteers

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
Hospital Universitario Virgen del Rocio
Coordinator of this site? Confirm its status
SevilleSpainUnknown status

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