Effect of Spirulina on Serum Hyaluronic Acid in Beta Thalassemic Children With Hepatitis C
NCT02744547 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2019-04-10
Summary
Thalassemics can develop liver fibrosis because of iron overload and hepatitis C infection. The latter is the main risk factor for liver fibrosis in transfusion dependent thalassemics. Excess liver iron is clearly recognized as a co factor for the development of advanced fibrosis in patients with hepatitis virus C infection. Hyaluronic acid serum levels correlate with histological stages of liver fibrosis in hepatitis C patients, so it has a good diagnostic accuracy as a non invasive assessment of fibrosis and cirrhosis.there is evidence that suggests Spirulina may help to protect against liver damage, cirrhosis and liver failure in those with chronic liver disease.
Conditions
- Beta Thalassemia Major
Interventions
- DIETARY_SUPPLEMENT
-
Spirulina
Spirulina in a dose of 250 mg/kg/day will be given orally for 3 months.
Sponsors & Collaborators
-
Tanta University
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 6 Years
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-12-31
- Primary Completion
- 2017-12-31
- Completion
- 2017-12-31
Countries
- Egypt
Study Locations
More Related Trials
-
Elastography vs Iron Regulators in the Diagnosis of Hepatic Fibrosis- Iron Overload in Children With Beta- Thalassemia
NCT07153926 ·Status: COMPLETED
-
Sperm DNA Damage in β-thalassemia Major: Is There a Role for Antioxidants?
NCT03014882 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
The Potential Hepatoprotective Effect of Metformin in Patients With Beta Thalassemia Major
NCT02984475 ·Status: UNKNOWN ·Phase: PHASE4
-
Benefits of Nigella Sativa in Children With Beta Thalassemia Major
NCT02816957 ·Status: UNKNOWN ·Phase: EARLY_PHASE1
-
Study of The Therapeutic Benefits of Al-hijamah in Children With Beta Thalassemia Major
NCT02761395 ·Status: UNKNOWN ·Phase: NA
-
The Effect of N-acetylcysteine on Oxidative Stress Status and Iron Overload in Thalassemia Major
NCT04260516 ·Status: COMPLETED ·Phase: PHASE1
-
Iron Status in BTM With Blood Transfusion
NCT04947540 ·Status: UNKNOWN
-
Clinical Study to Evaluate the Possible Efficacy and Safety of L- Carnitine and Sildenafil in Children Having Beta Thalassemia With Increased Tricuspid Regurgitant Jet Velocity
NCT05584956 ·Status: UNKNOWN ·Phase: PHASE3
-
Evaluation of the Free α-hemoglobin Pool in the Red Blood Cells : Prognostic Marker and Severity Index in Thalassemic Syndromes
NCT02855957 ·Status: COMPLETED ·Phase: NA
-
Hibiscus Sabdariffa and Centella Asiatica in the Treatment of Anemia by Iron Deficiency
NCT01414374 ·Status: COMPLETED ·Phase: PHASE3
-
The Change of Coagulation Markers in Children With β-thalassemia Disease After Stem Cell Transplantation
NCT00789516 ·Status: COMPLETED
-
Hydoxycarbamide and L-Carnitine Therapy in Sickle Cell Anemia
NCT05081349 ·Status: COMPLETED ·Phase: PHASE4
-
NAC Effect on Iron Overload and Blood Transfusion in β-thalassemia Major
NCT05777733 ·Status: UNKNOWN ·Phase: PHASE1
-
Hydroxy Urea, Omega 3, Nigella Sativa,Honey on Oxidative Stress and Iron Chelation in Pediatric Major Thalassemia
NCT04292314 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Liver Fibrosis in Sickle Cell Disease
NCT02007746 ·Status: COMPLETED
-
Assessment of Cognitive Function, Fatigue and Health Related Quality of Life in Children With Beta Thalassemia
NCT05469230 ·Status: COMPLETED
-
Effect of Incentive Respiratory Training on Pulmonary Functions and Functional Capacity in Children With B-thalassemia Major
NCT07112703 ·Status: RECRUITING ·Phase: NA
-
Safety and Pharmacokinetic Study of Escalating Doses of SP-420, an Iron Chelator, in Patients With β-Thalassemia
NCT02274233 ·Status: TERMINATED ·Phase: PHASE1
-
Correlation Between Pulmonary Functions and Physical Fitness in Children With β-thalassemia
NCT05494333 ·Status: UNKNOWN
-
Dermatological Abnormalities in Beta-thalassemia Major
NCT03894605 ·Status: UNKNOWN
-
Combination Therapy of Hydroxyurea With L-Carnitine and Magnesium Chloride in Thalassemia Intermedia
NCT00809042 ·Status: COMPLETED ·Phase: PHASE2
-
Hemoglobinopathy Nursing Program and Pediatric Nursing Students
NCT05389891 ·Status: COMPLETED ·Phase: NA
-
An Algorithm to Start Iron Chelation in Minimally Transfused Young Beta-thalassemia Major Patients
NCT02173951 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
Dental Dyschromia and Quality of Life in Early Prolonged Hyperbilirubinemia
NCT06506734 ·Status: RECRUITING
-
Efficacy and Safety of Efficacy and Safety of Continued Iron Chelation Therapy In Poly-transfused Thalassemia Patients With Low Serum Ferritin (< 500 ng/ml)
NCT01996683 ·Status: UNKNOWN ·Phase: NA