Clinical Trial Details
— Status: Not yet recruiting
Administrative data
| NCT number |
NCT03868306 |
| Other study ID # |
RCDWIVRCDWADGFIDAABTT |
| Secondary ID |
|
| Status |
Not yet recruiting |
| Phase |
|
| First received |
|
| Last updated |
|
| Start date |
June 1, 2019 |
| Est. completion date |
June 1, 2022 |
Study information
| Verified date |
March 2019 |
| Source |
Assiut University |
| Contact |
Ahmed Gad Al-Rab Askar, Professor |
| Phone |
00201010630005 |
| Email |
Hekma73[@]hotmail.com |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Observational
|
Clinical Trial Summary
Red Cell Distribution Width Index versus Red Cell Distribution Width as Discriminating Guide
for Iron Deficiency Anaemia and Beta Thalassemia Trait .
Description:
Microcytic hypochromic anaemia is very common hematological abnormality in the clinical
practice ( Snakar et;al. 2016 ) . Iron deficiency anaemia and beta thalassemia trait are the
most common causes of microcytic hypochromic anaemia. As mentioned by the World Health
Organization ( WHO ) estimates in 2004 , there were 273000deaths due to iron deficiency
anaemia along with 19.7 million disability . Approximately 1.3 % cases were recorded globally
in developing countries ( Kasseban et;al.2014 ) . Iron deficiency anemia is the most common
nutritional disorder . This type of anemia is the final phase of a process that begins with
exhaustion of iron stores and continues with iron depletion from other compartments that
contain it compromising normal haematopoesis ( Wharton et;al. 1994 ) Beta thalassemia trait
is the second most common cause of microcytic hypochromic anaemia . It is genetically
determined disorder in which the defect of b globin gene results in decreased production of
hemoglobin A1 ( Sliman et;al. 2004 ) The differentiation between Iron deficiency anemia and
Beta thalassemia trait is important because of two main reasons . First , because hemoglobin
will not improve in beta thalassemia trait if it is misdiagnosed as Iron deficiency anemia
and unnecessary iron being prescribed by the attending physician ( Vehapoglee et;al. 2014 ) .
The second grave reason is that misdiagnosed beta thalassemia trait as Iron deficiency anemia
may get married to a beta thalassemia trait , resulting in homozygous or thalassemia major in
the offsprings ( Tripathi et;al. 2015) Ideally one needs a battery of tests including
detailed peripheral blood picture , HBA2 estimation , serum iron , TIBC , serum ferritin and
transferrin saturation to differentiate Iron deficiency anemia from beta thalassemia trait
clearly (Bordbar et;al. 2015 ) . But all these investigations are either not available in all
clinical setup or they are relatively time consuming and need expensive techniques ( Natios
et;al. 2007 ). Derived indices showed that RDW is the first index of the routine blood count
to become abnormal during the development of Iron deficiency anemia ( McCulre et;al. 1985 ) .
It quantitatively measures red blood cells size.
variation computed directly from the RBCs histogram and is calculated as standard statistical
value , the coefficient of variation of the volume distribution ( Verma et;al. 2015 and
Plengsures et;al. 2015) . RDW is high in Iron deficiency anemia because there is a wide
variation in red cell size . in beta thalassemia trait , the red cells are all the same size
, there is virtually no variation ,so RDW is low ( Park et;al.2009 ) . Another red cell
discriminate function , RDWI had been proven to be reliable discrimination index in the
differentiation between Iron deficiency anemia and beta thalassemia trait ( Ismail et;al.2016
) . It can be easily calculated as ( MCV in ( Fl) x RDW / RBCs in (million per microlitre ) )
quotient more than 220 suggest Iron deficiency anemia
, less than 220 suggest beta thalassemia trait. RDWI provide valiable help to the attending
physician as all discriminating factors including RBCs count , MCV and RDW are incorporated
in its formula ( Jayabose et;al. 1999 ) .
