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NCT07157722Not yet recruitingPhase 3

Evaluating the Effect of N-Acetyl Cysteine and Alpha Lipoic Acid in Patients With Beta Thalassemia

The Potential Role of N-Acetyl Cysteine or Alpha-Lipoic Acid as Adjuvant Therapies in the Treatment of Patients With Beta Thalassemia

Source: ClinicalTrials.gov · Last updated 5 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The current study is to investigate the potential roles of N-acetyl cysteine and Alpha-lipoic acid in patients with beta-thalassemia.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
66 (estimated)
First submitted
28 Aug 2025
Start date
30 Aug 2025
Primary completion date
30 Dec 2025
Lead sponsor
Tanta University
Diseases
Thalassaemia
NCT number
NCT07157722

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 66
  • From 30 Aug 2025 to the primary completion date, 30 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients with a prior history of significant cardiovascular diseases, such as coronary artery disease, myocardial infarction, or stroke.
  • Patients who will be non-compliant with the prescribed therapy.
  • Patients who will receive antioxidant or anti-inflammatory medications.

Other illness

  • Patients with familial hypercholesterolemia or history of premature atherosclerosis.
  • Patients with diabetes.
  • Patients with inflammatory diseases, such as Systemic lupus erythematous, rheumatoid arthritis and inflammatory bowel disease.
  • Patients with oxidative stress related diseases, such as Alzheimer, Parkinson, COPD and cancer.

Other

  • Patients with severe renal dysfunction.
  • Patients with severe hepatic dysfunction.
  • Patients with other hemoglobinopathies.
  • Pregnant women.
  • Obese patients.

Who the study is looking for

  • Patients with beta-thalassemia who will receive conventional thalassemia management.
  • Both genders.
  • Age ≥ 18 years old.

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Faculty of Pharmacy, Tanta University
Coordinator of this site? Confirm its status
TantaEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.