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RecruitingNCT05979675AMLREGISTRYUpdated Aug 7, 2023

Acute Myeloid Leukemia Registry

An observational study in Acute Myeloid Leukemia, sponsored by Turkish Hematology Association. Recruiting at 1 site in Turkey. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-08-07.

Sponsored by Turkish Hematology Association · Observational

From the registry’s dates

  • Started Dec 2021; still recruiting 4 years 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
250
Ages
18 Years and older
Sex
All
01

Study summary

All acute myeloid leukemia (AML) patients diagnosed after 1 Jan 2020 will be included to this study.

Read the detailed description

This is a non interventional prospective disease registry, 250 prospective patients diagnosed with AML across 20 centers in Turkey.

Participating sites will consist of hematology clinics and routine follow-up procedures will be followed-up.

All patients diagnosed after 1 Jan 2020 as AML will be included and patients will be enrolled during 24 months of period and will be followed-up 36 months. Study will be completed in 60 months.

02

Conditions studied

03

In context

Leukemia

5,441 studies on the registry are indexed under Leukemia; 637 are open to participants now.

This study's planned enrollment of 250 is above the median of 120 across 744 observational studies indexed under Leukemia.

Browse Leukemia studies →

Lead sponsor

Turkish Hematology Association is the lead sponsor of 3 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All AML patients diagnosed after 1 Jan 2020 will be included to this study.

Inclusion criteria

  • Diagnosed as AML after 1 Jan 2020
  • Patients signed informed consent form

Exclusion criteria

Exclusion Criteria:

  • Patients under 18 years old
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
250 participants (estimated)
Target follow-up
24 Months
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. Overall Survival

    From diagnosis to exits by any cause

    Time frame: 60 months

07

Study locations

1 of 1 sites recruiting
  • Antalya Training and Research Hospital
    Antalya, Turkey
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 7, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05979675
Lead sponsor
Turkish Hematology Association
Responsible party
Sponsor
First posted
Aug 7, 2023
Start date
Dec 21, 2021
Primary completion
Dec 21, 2026 (estimated)
Completion
Dec 21, 2026 (estimated)
Last update
Aug 7, 2023

Study contacts

Volkan Karakus, Assoc. Prof.
Contact
dr_v_karakus@yahoo.com
905057656778
Ilker Kurkcu
Contact
ilker.kurkcu@sentez-cro.com
905326354515
Ilker Kurkcu
study director · Sentez Cro

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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