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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT01416311
Date of registration: 09/06/2011
Prospective Registration: No
Primary sponsor: Novartis Pharmaceuticals
Public title: Drug Use Investigation for REVOLADE (ITP)
Scientific title: Drug Use Investigation for REVOLADE (Chronic Idiopathic Thrombocytopenic Purpura)
Date of first enrolment: December 21, 2010
Target sample size: 5797
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT01416311
Study type:  Observational
Study design:   
Phase: 
Countries of recruitment
Contacts
Name:     Novartis Pharmaceuticals
Address: 
Telephone:
Email:
Affiliation:  Novartis Pharmaceuticals
Key inclusion & exclusion criteria

Inclusion Criteria:

- Subjects with chronic idiopathic thrombocytopenic purpura

Exclusion Criteria:

- Not applicable



Age minimum: N/A
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Purpura, Thrombocytopaenic, Idiopathic
Intervention(s)
Drug: Eltrombopag
Primary Outcome(s)
The number of subjects with any adverse events treated with REVOLADE [Time Frame: 1 year]
Secondary Outcome(s)
Appearance of thromboembolism [Time Frame: 1 year]
Secondary ID(s)
114877
CETB115B1401
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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