Actively Recruiting
Role of Eltrombopag as First Line Therapy in Primary Immune Thrombocytopenia.
Led by Renata PLC · Updated on 2025-02-18
100
Participants Needed
1
Research Sites
46 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This will be a double-blind, placebo-control, randomized clinical trial conducted in the Department of Hematology, DMCH for one year. This study will help to establish the role of eltrombopag as a first-line therapy in newly diagnosed ITP. Newly diagnosed ITP patients will be selected after meeting inclusion and exclusion criteria, they will be thoroughly informed about the study, used drugs, randomization, risks, benefits, and follow-up. If they agree to participate, their consent will be taken and they will be enrolled in the study. A detailed history and clinical exam will be done. Primary investigation will be - CBC PBF, RBS, ANA, TSH, Anti H. pyloriIgG, Anti-HCV, APTT, and BMS (if indicated). The main outcome variable will be platelet count and number of spontaneous bleeding. Total sample size would be 100 (50 in each group). Enrolled patients would be divided into two groups (1:1) by block randomization. One group will get Eltrombopag\& Prednisolone and other group will get Eltrombopag\& Placebo. Researchers or any one related to the study in DMCH, patients \& their attendants, no one will know which patient will get placebo or eltrombopag. Only a respectable third party will know the information. A patient would be followed up on 1st, 2nd and 4th week of starting therapy. Patients would be evaluated in every follow up by history, physical examination and investigation. History of any spontaneous bleeding event, any discomfort or new symptoms science last follow up will be noted. General examination will be performed in every follow-up. CBC, RBS, ALT, AST, creatinine will be done in every follow-up. Data will be collected on a pre-designed case record form and will be collected through face-to-face interviews, physical examination, and laboratory reports. After data collection data will be edited, cleaned, and prepared for analysis at the end of the study. The statistical analysis will be conducted using SPSS version 25 statistical software. The results of the study will be published in national and international journals.
CONDITIONS
Official Title
Role of Eltrombopag as First Line Therapy in Primary Immune Thrombocytopenia.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with newly diagnosed ITP
- Platelet Count �30x10�9/L or less
- Age between 18 to 70 years
You will not qualify if you...
- Persistent or chronic ITP
- Pregnant women
- Secondary ITP due to SLE, Anti-phospholipid syndrome, Evans syndrome, HCV or H Pylori associated ITP
- History of vaccination, recent viral infection, or fever
- Evan's Syndrome
- Known chronic renal failure or liver diseases
- Grade 3 or 4 bleeding at presentation
AI-Screening
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Trial Site Locations
Total: 1 location
1
Dhaka Medical College Hospital
Dhaka, Bangladesh, 1000
Actively Recruiting
Research Team
M
Md Manirul Islam, MBBS,FCPS
CONTACT
G
Gazi Yeasinul Islam, MBBS,FCPS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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