CTRI/2024/06/068935Not yet recruitingPhase 3
Comparative study for efficacy of L-carnitine and N-acetyl cysteine on iron overload induced oxidative stress in patients with thalassemia: A Randomized Control Trial - NI
Dr Pragna Roy0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 3
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1)Patients with thalassemia on blood transfusion
- •2)Patients or legally authorized representative willing to give informed consent and assent for the trial.
Exclusion Criteria
- •1)Patients with history of allergic reactions attributed to compounds of similar chemical or biologic composition of N-Acetyl-Cysteine and L-Carnitine
- •2)Patients with history of central nervous system diseases (like epilepsy, psychiatric disorder) or taking any medicine for such illness.
- •3)Patients with history of severe renal or hepatic disease (like hepatitis B or C)
- •4)Patients with history of bronchospastic diseases (like asthma)
- •5)Patients with history of hypothyroid disorder
- •6)Patients on warfarin or acenocoumarin therapy
Investigators
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