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Not yet recruitingNCT06708728Updated Nov 27, 2024

Study of Acquired Hemolytic Anemia in Adult Hospitalized Patients

An observational study in Hemolytic Anemia, sponsored by Sohag University. Not yet recruiting at 1 site in Egypt. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-11-27.

Sponsored by Sohag University · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2025, 1 year 5 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
60
Ages
18 Years and older
Sex
All
01

Study summary

the goal of the study is to identify the most common etiological factors and analyze the clinical presentations and laboratory findings in hospitalized patients with acquired hemolytic anemia associated with non-neoplastic diseases.

And to evaluate short-term outcomes, including morbidity and mortality rates, and to determine correlations between specific etiological factors and patient outcomes in these cases.

02

Conditions studied

  • Hemolytic Anemia

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03

In context

Anemia, Hemolytic

56 studies on the registry are indexed under Anemia, Hemolytic; 16 are open to participants now.

This study's planned enrollment of 60 is close to the median of 56 across 16 observational studies indexed under Anemia, Hemolytic.

Browse Anemia, Hemolytic studies →

Lead sponsor

Sohag University is the lead sponsor of 1,230 studies on the registry; 636 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

patients admitted in Internal Medicine department and Intermediate care unit at sohag university hospital

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults aged 18 years and older.
  • Patients diagnosed with acquired hemolytic anemia.
  • Patients must be hospitalized in the Internal Medicine department at the time of diagnosis of acquired hemolytic anemia during the study period
  • Patients (or their legal representatives) must provide informed

Exclusion criteria

Exclusion Criteria:

  • Patients with underlying neoplastic diseases.
  • Patients with hereditary hemolytic anemia.
  • Patients or their representatives who do not consent to participate in the study.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
60 participants (estimated)
Patient registry
No

Interventions

  • Otherblood samples

    blood samples for CBC parameters , peripheral blood smear, bilirubin levels and kidney function tests

06

What researchers measure

Primary outcomes

  1. intensive care unit admission of the patients due to progression of the disease complications.

    Primary outcome will be ICU admission due to progression of the disease complications.

    Time frame: through study completion, an average of 6 months

Secondary outcomes

  1. mortality within duration of hospital admission

    Secondary outcome will be mortality within duration of hospital admission

    Time frame: through study completion, an average of 6 months

07

Study locations

1 site
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Dec 2024; primary completion for Jun 2025, 6 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 22, 2024
First posted
Nov 27, 2024
StartEst.
Dec 2024
Primary completionEst.
Jun 2025
CompletionEst.
Jun 2025
Last update
Nov 27, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 27, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06708728
Lead sponsor
Sohag University
Responsible party
Ahmed Elsayed Mahmoud (resident doctor, Sohag University) — Principal investigator
First posted
Nov 27, 2024
Start date
Dec 2024 (estimated)
Primary completion
Jun 2025 (estimated)
Completion
Jun 2025 (estimated)
Last update
Nov 27, 2024

Study contacts

Ahmed E Mahmoud
Contact
ahmed.elsayed95@med.sohag.edu.eg
02 01145943157
Mahmoud I Yousef, Lecturer of Internal Medicine
Contact
02 0106 596 4083

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2024. You cannot join it, but the record below documents what was studied.

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Discussion

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