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Study of The Therapeutic Benefits of Al-hijamah in Children With Beta Thalassemia Major

Study of The Therapeutic Benefits of Al-hijamah in Children With Beta Thalassemia Major

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02761395
Acronym
Al-hijamah
Enrollment
60
Registered
2016-05-04
Start date
2015-11-30
Completion date
2017-05-31
Last updated
2017-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

AL-Hijama in Thalassmia Major

Brief summary

1. Evaluate the therapeutic effects, health benefits, and immunological effect of Al-hijamah in children with beta thalassemia major. 2. Evaluate the extent of clinical improvement, reductions in serum iron and ferritin, antioxidant status, in those patients.

Detailed description

The present study will be carried on 60 children patients with β- thalassemia major attending The Hematology Unit of Paediatric Departments at Tanta University Hospital. Participants will divide into 3 groups: Group 1: 20 patients receive Al-hijamah. Group 2: 20 patients receive Al-hijamah plus iron chelation therapy. Group 3: 20 patients receive iron chelation therapy only Participants undergo: 1. Laboratory investigations: * CBC (complete blood count) of peripheral venous blood before Al-hijamah and daily after it. * Differences between CBC from venous blood and cupped blood (bloody excretion collected inside suction cups). Cupped blood is collected in heparin coated with and added to suction cups put on the skin surface. • Serum iron and ferritin before Al-hijamah and after it. • Serum iron and ferritin in cupped blood vs venous blood. • Serum lipid profile and glycosylated hemoglobin before Al-hijamah and after it. * Total antioxidant capacity and some serum oxidants e.g. malondialdehyde before and after treatment * Flow cytometric analysis of number of Natural killer cells, CD4 T helper cells and CD4/CD8 cells (optional) (cluster of differentiation). They were reported to improve markedly after Al-hijamah. * Estimating serum LDH, pyruvate (antioxidant) and lactate (metabolite of pyruvate through LDH) in thalassemia patients before and after Al-hijamah 2. Assessment of heart function by Echocardiographic study (before and 3 month after Al-hijamah): * lines of therapy: Technical steps of Al-hijamah (Necessary equipments are ready and can do it for all patients if possible): Al-hijamah (Triple S technique under strict sterilization): * Strict sterilization of selected anatomical sites. * Suction using sterile plastic disposable sucking cups * Skin scarifications (shartat mihjam): through inducing superficial (0.1 mm in depth), small (2 mm in length), multiple and evenly distributed skin incisions. * Suction using sterile plastic disposable sucking cups * Strict sterilization of selected anatomical sites. Study endpoint: This study will be terminated if safety of the patient were in dangers due to elements related to the new therapeutic agent or if the treatment not proven efficacious. 5\. Risks to participants are reasonable in relation to anticipated benefits. Many human studies have proven safety of Al-hijamah. 6\. Compensations of controls for transportation or work absence and of patients for any injury, and if so, description of the compensation should be mentioned. No, compensations. 7\. The proposal include a clear statement that an informed consent will be obtained from all participants in this research.

Interventions

PROCEDUREAl-hijamah

* Strict sterilization of selected anatomical sites. * Suction using sterile plastic disposable sucking cups * Skin scarifications (shartat mihjam): through inducing superficial (0.1 mm in depth), small (2 mm in length), multiple and evenly distributed skin incisions.

DRUGDeferasirox

20-40 mg/kg/day orally

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
4 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Children suffering from beta thalassemia major, with age range from 4-18 years.

Exclusion criteria

* Children with Congenital heart disease * Children with Rheumatic heart disease * Presence of heart failure * Children with Coronary arterial disease * Children with Cardiomyopathy * Children with hypotension * Children with inflammatory skin diseases e.g. acute burns

Design outcomes

Primary

MeasureTime frameDescription
CD(cluster of differentiation)4 and CD8 count3monthcount and percentage

Secondary

MeasureTime frameDescription
serum levels of cholesterol and triglyceride3monthlevel of cholesterol and triglyceride (mg per dl)
alanine amino transferase , aspartate amino transferase3monthmeasured as unit per litre
serum ferritin3 monthsmeasured as ng per dl
malodialdehyde ant total antioxidant capacity3 monthsmeasuedas mmol per litre

Countries

Egypt

Contacts

Primary ContactNahed Habas, MD
nahedhablas79@gmail.com01010560350
Backup ContactMohammed El shanshoryR, Prof.
elshanshory@hotmail.com01005680834

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026