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NCT07835282Not yet recruiting

Germany on Target Registry

Source: ClinicalTrials.gov · Last updated 28 Sept 2026

Brief summary (registry, in English)

Germany on Target Registry (DaZiR) is a prospective, Germany-wide patient registry designed to assess lipid management and low-density lipoprotein cholesterol ( LDL-C) target attainment in adults following acute myocardial infarction (STEMI or NSTEMI). Eligible patients are informed about the registry by treating physicians or their medical teams and receive an individual access link or QR code. Following electronic informed consent and registration, participants provide clinical and follow-up information through the brite™ platform. Clinical data, including LDL-C values and lipid-lowering treatment, can be entered by the participants or obtained from uploaded medical documents. The platform enables participants to follow the course of their LDL-C values and provides reminders for scheduled follow-up data collection. Medical treatment is determined independently by the treating physicians as part of routine clinical care and is not assigned by the registry. The registry aims to assess LDL-C target attainment over time, changes in lipid-lowering treatment, treatment adherence and cardiovascular outcomes following myocardial infarction.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
10000 (estimated)
First submitted
10 Sept 2026
Start date
1 Dec 2026
Primary completion date
1 Jan 2036
Lead sponsor
Deutsche Gesellschaft für Lipidologie e. V. (DGFL) - Lipid-Liga
NCT number
NCT07835282

What you commit to

  • Study type: Observational
  • Planned participants: 10000
  • From 1 Dec 2026 to the primary completion date, 1 Jan 2036
  • No sites listed in no 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

  • No informed consent for participation in the registry

Who the study is looking for

  • Age ≥18 years
  • Diagnosis of acute ST-elevation myocardial infarction (STEMI) or non-ST- elevation myocardial infarction (NSTEMI)
  • Provision of informed consent for participation in the registry

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

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