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Recruiting NCT03188874

NCT03188874 Clinical AML Registry and Biomaterial Database of the Study Alliance Leukemia (SAL)

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Clinical Trial Summary
NCT ID NCT03188874
Status Recruiting
Phase
Sponsor Technische Universität Dresden
Condition Acute Myeloid Leukemia (AML)
Study Type OBSERVATIONAL
Enrollment 15,000 participants
Start Date 2010-09
Primary Completion 2030-09-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 15,000 participants in total. It began in 2010-09 with a primary completion date of 2030-09-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This is a registry study in adult patients with newly diagnosed or refractory/relapsed acute myeloid leukemia. Investigator's sites: 60 sites in Germany. Primary objectives: * Identification of epidemiological data on AML: age, prognostic factors and subgroup distributions. Incidence and age distribution are compared with the data of population-related tumor registry. * Evaluation of the most important patient-relevant clinical endpoints (outcomes): relapse-free survival (RFS) / time to relapse (TTR), calculation of cumulative incidence of relapse (CIR) and overall survival (OS) * Documentation of treatment strategy

Eligibility Criteria

Inclusion Criteria: * AML according to the WHO (World Health Organization) diagnostic criteria, including acute promyelocytic leukemia * Age ≥ 18 years. There is no upper age limit. * Signed written informed consent Exclusion Criteria: * there are no exclusion criteria

Contact & Investigator

Central Contact

Christoph Röllig, Prof. Dr.

✉ christoph.roellig@uniklinikum-dresden.de
Principal Investigator

Christoph Röllig, Prof. Dr.

STUDY DIRECTOR

Universitätsklinikum Carl Gustav Carus

Frequently Asked Questions

Who can join the NCT03188874 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Acute Myeloid Leukemia (AML). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT03188874 currently recruiting?

Yes, NCT03188874 is actively recruiting participants. Contact the research team at christoph.roellig@uniklinikum-dresden.de for enrollment information.

Where is the NCT03188874 trial being conducted?

This trial is being conducted at Baden-Baden, Germany, Heidelberg, Germany, Mannheim, Germany, Schwäbisch Hall, Germany and 11 additional locations.

Who is sponsoring the NCT03188874 clinical trial?

NCT03188874 is sponsored by Technische Universität Dresden. The principal investigator is Christoph Röllig, Prof. Dr. at Universitätsklinikum Carl Gustav Carus. The trial plans to enroll 15,000 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology