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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02816957
Other study ID # 30794l03l16
Secondary ID
Status Recruiting
Phase Early Phase 1
First received June 23, 2016
Last updated April 24, 2017
Start date June 2016
Est. completion date June 2017

Study information

Verified date June 2016
Source Tanta University
Contact Nahed Mohamed Habas, MD
Phone 01010560350
Email nahedhablas79@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluate the therapeutic effects health benefits, and immunological effect of Nigella sativa in children with beta thalassemia major.


Description:

Study will be carried on children patients with β- thalassemia major attending The Hematology Unit of Pediatric Department at Tanta University Hospital. patients are divided into 2 groups: patients in the control group, patients in the treatment group that will receive nigella sativa powder for 3 consecutive months. Then Evaluate the therapeutic effects health benefits, and immunological effect of Nigella sativa in children with beta thalassemia major.

Evaluate the extent of clinical improvement, reductions in serum iron and ferritin, antioxidant status, treatment of the causes of hemolysis and other therapeutic benefits of Nigella sativa in those patient.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date June 2017
Est. primary completion date June 2017
Accepts healthy volunteers No
Gender All
Age group 3 Years to 18 Years
Eligibility Inclusion Criteria:

- Thalassemia with iron overload

Exclusion Criteria:

- Thalassemia complicated with diabetes mellitus or hepatitis

- Patients who discontinue treatment

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
nigella sativ
nigella sativa powder (2 gm/day) for 3 consecutive months.

Locations

Country Name City State
Egypt Faculty of Medicine- Tanta University Tanta Gharbia

Sponsors (1)

Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary malondialdehyde nmol serum level of malondialdehyde (nmol per liter) 3 months
Primary cluster of differentation4 and 8(CD4 and CD8) CD4 and CD8 cell per cmm 3 months
Primary total antioxidant total antioxidant(mmol per liter) 3 months
Secondary Serum iron microgram per dl 3 months
Secondary total iron binding capacity microgram per dl 3 months
Secondary serum ferritin ng per ml 3 months
Secondary complete blood count complete blood count 3 months