AzTrials
AzTrials

Beta Thalassemia Major AnemiaPhase 4NCT02984475

The Potential Hepatoprotective Effect of Metformin in Patients With Beta Thalassemia Major

A Phase 4 study testing Metformin in people with Beta Thalassemia Major Anemia, run by Cairo University at 2 sites in Egypt.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

Beta Thalassemia is a major public health problem in Mediterranean countries.In Egypt, it is considered as the most common chronic hemolytic anemia.one of the major complications in this inherited disorder is iron overload which lead to oxidative stress and tissue damage. Read more about this study

Who is it for?
Ages 11 to 18 years
Conditions the study is for
Beta Thalassemia Major Anemia
What is being tested?
Metformin
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
2 sitesEgypt
Study dates
Dec 2016to Apr 2019
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 11 to 18 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • Diagnosed with Beta-Thalassemia Major and receiving regular blood transfusion and on iron chelating therapy.
  • Weight: equal to or over 35 kg.
  • Normal renal function.

Who cannot join

  • Patients with renal impairment (serum creatinine more than twice the upper limit of normal).
  • Patients with heart failure.
  • Patients with sepsis or active infection.
  • Patients with diabetes mellitus (either primary or secondary to thalassemia).
  • regular consumption of medication with potential hepatotoxicity.
  • regular herbal medicine or antioxidant supplementation.
  • patients with gastrointestinal conditions preventing adsorption of oral medication.

Trial locations and contacts

2 sites in 1 country.

Egypt2 sites, 1 recruiting
  • Abo El Reesh Hospital

    Cairo

    Mona Gaber, Bachelor., 0223648368, mona.sobhy@pharma.cu.edu.eg

    Recruiting
  • El Demerdash (Ain Shams Teaching Hospital).

    Cairo

    Completed

Other trials in Egypt

About this study

Official title: The Potential Hepatoprotective Effect of Metformin in Patients With Beta Thalasemia Major

Beta Thalassemia is a major public health problem in Mediterranean countries.In Egypt, it is considered as the most common chronic hemolytic anemia.one of the major complications in this inherited disorder is iron overload which lead to oxidative stress and tissue damage.

Regarding toxic effect of iron overload on liver, hepatomegaly is one of the most findings that resulting from hemosiderosis, extra medullary hematopoiesis, transmitted hepatitis B and C and cirrhosis.

Read more

A lot of studies have been carried out recently to study the beneficial role of metformin in non-diabetic patients of different disorders as non-alcoholic fatty liver disease (NAFLD).Among several studies, it's demonstrated that metformin significantly improved insulin resistance, aminotransferase levels and liver morphology.

The role of metformin in these studies is mainly thought to be antioxidant and anti-inflammatory effects. However, the role of Metformin on hepatic function in different populations with the same mechanism of liver injury should be further investigated.

This clinical trial will be carried out on 60 patients with beta thalassemia major receiving regular blood transfusion and iron chelating therapy, either HCV positive or negative patients.

They will be randomly distributed into either control group (group 1, n=30) receiving blood transfusion and taking iron chelating therapy or treatment group (group 2, n=30) receiving blood transfusion and taking iron chelating therapy along with metformin tablets (500 mg/twice daily) for 6 months.

Read the detailed description

Beta-Thalassemia is a major public health problem in Mediterranean countries , parts of North and West Africa, the Middle East, the Indian subcontinent, southern Far East and southeastern Asia is of the highest incidence. In Egypt, it is considered as the most common chronic hemolytic anemia (85.1%) with 5.3- 9% carrier rate and annual birth of 1000/1.5 million live births. Thalassemia is a heterogeneous group of hereditary anemia that results from reduced or absent production of alpha or beta globin chains of hemoglobin A. β-thalassemia patients have partial or complete lack of production of β-chains of hemoglobin. The remaining excess of α-chains are unstable, and they finally precipitate and disintegrate, causing red blood cell (RBC) membrane damage. The affected RBCs are prematurely hemolysed in the spleen and bone marrow, leading to increased RBC turnover, ineffective erythropoiesis, and severe anemia that can only be controlled by regular blood transfusion.

One of the major complications in this inherited disorder is iron overload because of premature hemolysis, ineffective erythropoiesis and repeated transfusion in the plasma and major organs such as heart, liver, and endocrine glands. Iron has a catalytic role to produce powerful reactive oxidant species (ROS) and free radicals, which lead to oxidative stress and damage . Children with beta thalassemia have oxidative stress and antioxidant deficiency even without iron overload status. The only way to avoid the accumulation of potentially toxic iron is iron chelation along with the transfusional therapy, desferrioxamine is a chelating agent that has been discovered 30 years ago and since then it has been considered to be one of the most important chelating agent that have been extensively used in the clinical practice . Then other iron chelating agents have been discovered as deferasirox (Exjade®) and deferiprone (Kelfer®). However, there are a lot of problems regarding the compliance to desferrioxamine regimen and the side effects of other orally active iron chelating agents, which rises the need for studying the effect of other naturally occurring iron chelating agents and supplements to reduce the consequences of the iron overload. As reactive oxygen species (ROS) and iron overload have an important role in the pathophysiology of thalassemia , some studies have been carried out to determine the effects of supplements such as silymarin and vitamin E in thalassemic patients on regular blood transfusion and desferrioxamine, and they showing benefit due to their antioxidant, cytoprotective, and iron-chelating activities .

Regarding the toxic effect of iron overload on liver, hepatomegaly is one of the most findings that resulting from hemosiderosis, extra medullary hematopoiesis, transmitted hepatitis B and C and cirrhosis . In one study, liver function tests (LFT) and serum ferritin were elevated in most patients in spite of desferoxamine use .

Metformin (Biguanides) is used as a first-line treatment for patients with type 2 diabetes mellitus . But it is not the only use of metformin, a lot of studies have been carried out recently to study the beneficial role of metformin in non-diabetic patients of different disorders. Metformin was shown to be safe and effective for management of type 2 diabetes in pediatric patients aged 10-16 years old, initiated dose of 500 mg twice daily and titrated up to a maximum of 2000 mg/day based on response . Several clinical studies have supported the beneficial role of metformin in patients with non-alcoholic fatty liver disease (NAFLD) . Most of these studies have evaluated the effect of different doses of metformin on liver biochemistry (aminotransferase profile), histology, and metabolic syndrome feature . Among several studies, it's demonstrated that metformin significantly improved insulin resistance, aminotransferase levels, and liver morphology. Furthermore, in ob/ob mice, a model of hepatic steatosis, it has been shown that metformin reversed hepatomegaly, hepatic fat accumulation, and ALT abnormalities, by reducing hepatic tumor necrosis factor-α (TNF-α) expression . Also the hepatoprotective effect of metformin on methotrexate-induced hepatotoxicity in rabbits with acute lymphocytic leukemia (ALL) has been established. The role of metformin in these studies is mainly thought to be antioxidant and anti-inflammatory effects. However, the role of Metformin on hepatic function in different populations with the same mechanism of liver injury should be further investigated.

This study is conducted to determine the safety and efficacy of metformin as hepatoprotective and antioxidant therapy in iron overloaded patients with Beta-Thalassemia Major.

Being tested
Metformin
Keywords
Beta Thalassemia, Metformin, Oxidative stress, Iron overload, Liver function
Medical subject headings
beta-Thalassemia, Iron Overload

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT02984475
Study groupRoleWhat they receive
treatment armActive comparator30 patients receiving blood transfusion and taking iron-chelating therapy along with metformin tablets (500 mg once daily for the first week then twice daily for 6 months).
Receives: Drug: Metformin
control armNo intervention30 patients receiving blood transfusion and taking iron-chelating therapy.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. liver enzymes tests.

    Alanine aminotransferase (ALT) and Aspartate aminotransferase (AST).

    Measured: 6 months

Secondary outcomes (8)
  1. Metformin Safety - Number of participants with treatment-related adverse events

    Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

    Measured: 6 months

  2. liver enzymes and function tests - Alkaline phosphatase (ALP).

    Alkaline phosphatase (ALP).

    Measured: 6 months.

  3. liver enzymes and function tests - Gama-Glutamyl transferase (GGT).

    Gama-Glutamyl transferase (GGT).

    Measured: 6 months.

  4. liver enzymes and function tests - total and direct bilirubin.

    total and direct bilirubin.

    Measured: 6 months.

  5. liver enzymes and function tests - Albumin.

    Albumin .

    Measured: 6 months.

  6. liver enzymes and function tests - International Normalized Ratio (INR).

    International Normalized Ratio (INR).

    Measured: 6 months.

  7. oxidative stress markers (MDA).

    Malondialdehyde (MDA)

    Measured: 6 months.

  8. oxidative stress markers (TAC).

    Total antioxidant capacity (TAC).

    Measured: 6 months.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Dec 2016 (estimated)
  2. Study startDec 2016
  3. Primary completionDec 2018 (estimated)
  4. Study completionApr 2019 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02984475
Sponsor's protocol ID
CL 1726
Status last verified
Jul 2018
First submitted
25 Nov 2016
Last updated
18 Jul 2018
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Metformin in people with Beta Thalassemia Major Anemia, run by Cairo University at 2 sites in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 18 Jul 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

liver enzymes tests. (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Jul 2018.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in