CClinicalTrials.gg
CompletedNCT00971698Updated Aug 26, 2011

The Spleen in Sickle Cell Anemia and Sickle Cell Thalassemia

An observational study in Sickle Cell Anemia and Thalassemia, sponsored by HaEmek Medical Center, Israel. Completed at 1 site in Israel. Open to participants aged 1 Year to 35 Years. Per ClinicalTrials.gov, last updated 2011-08-26.

Sponsored by HaEmek Medical Center, Israel · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
50
Ages
1 Year to 35 Years
Sex
All
01

Study summary

The spleen in Sickle Cell Anemia and Sickle Cell Thalassemia is usually enlarged in the first years of life but the immune protection provided is considered insufficient. In homozygous Sickle cell patients the spleen usually developed recurrent infarcts and after the first decade of age become fibrotic. Acute splenic sequestration is also frequent in those patients and this is considered as an indication for splenectomy.

In comparison in Sickle cell thalassemia patients, hypersplenism is more frequent.

The purpose of this study is to compare the clinical and laboratory issues related to the spleen in two groups of Sickle cell patients.

Read the detailed description

Clinical and laboratory characteristics related to the spleen in SCA patients will be studied.

Two groups of patient will be compared, a group of Sickle cell patients (Homozygous) and a second group of patients with Sickle cell beta thalassemia.

In those patients that splenectomy was performed the incidence of infections will be recorded besides the indications for splenectomy and the incidence of thrombotic events or thrombocytosis.

02

Conditions studied

  • Sickle Cell Anemia
  • Thalassemia

Keywords

  • Splenectomy
  • Thrombocytosis
  • Infections
  • Spleen
  • Sickle Cell Thalassemia
03

In context

Anemia

1,733 studies on the registry are indexed under Anemia; 246 are open to participants now.

This study's planned enrollment of 50 is below the median of 200 across 326 observational studies indexed under Anemia.

Browse Anemia studies →

Lead sponsor

HaEmek Medical Center, Israel is the lead sponsor of 228 studies on the registry; 12 are open to participants now.

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

04

Who can participate

Ages eligible
1 Year to 35 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Two groups of patients: 25 patients with homozygous Sickle Cell Anemia and 25 patients with Sickle Cell Thalassemia

Inclusion criteria

  • All the patients followed up at the Pediatric Hematology Unit

Exclusion criteria

Exclusion Criteria:

  • Patients lost from follow up of with insufficient data
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
50 participants (estimated)

Groups and cohorts

  • Sickle Cell Patients

    Patients with homozygous Sickle Cell Anemia

  • Sickle Cell Thalassemia

    Patients with Sickle Cell Thalassemia

06

What researchers measure

Primary outcomes

  1. Clinical events and abnormal laboratory results

    Time frame: One year

07

Study locations

1 site
  • Pediatric Hematology Unit and Pediatric Dpt B - HaEmek Medical Center
    Afula, 18101, Israel
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 26, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00971698
Lead sponsor
HaEmek Medical Center, Israel
Responsible party
Dr Koren Ariel (Head of Pediatric Hematology Unit and Pediatric Dpt B, HaEmek Medical Center, Israel) — Principal investigator
First posted
Sep 4, 2009
Start date
Feb 2009
Primary completion
Aug 2010
Completion
Aug 2010
Last update
Aug 26, 2011

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2011. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion