Efficacy of Helicobacter Pylori Eradication, Anti-D and Danazol Combination in Steroid Dependant or Refractory Immune Thrombocytopenia (ITP)
Primary Purpose
Thrombocytopenia
Status
Unknown status
Phase
Phase 2
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Steroid refractory ITP
Sponsored by
About this trial
This is an interventional treatment trial for Thrombocytopenia focused on measuring ITP
Eligibility Criteria
Inclusion Criteria:
1.ITP is defined by
- (a) a true thrombocytopenia on blood smear, (b) adequate megakaryopoiesis on bone marrow examination, (c) the absence of clinically apparent associated conditions or cause of thrombocytopenia
- 2.Steroid dependant ITP: more than 10 mg of prednisolone per day is required to maintain a platelet count above 20X109/L (minimum follow up duration: 3 months after diagnosis)
- 3.Steroid refractory ITP: a platelet count less than 20X109/L despite of treatment with full dose of steroid (prednisolone 1mg/kg for at least 4 weeks)
- 4.18 years old or more
Exclusion Criteria:
- 1.Patients who have a cause of thrombocytopenia such as HIV infection, lymphoproliferative disease, liver disease, definite SLE or drug
- 2.Pregnancy
- 3.Splectomized patients
- 4.Rh- blood type
- 5.Hemoglobin < 10g/dL
- 6.Known hypersensitivity to immunoglobulins
- 7.A positive direct antiglobulin test
- 8.Clinically relevant hepatic or renal disease
Sites / Locations
- Asan Medical CenterRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Steroid dependant ITP
Arm Description
more than 10 mg of prednisolone per day is required to maintain a platelet count above 20X109/L (minimum follow up duration: 3 months after diagnosis)
Outcomes
Primary Outcome Measures
Proportion who would avoid splenectomy at 6 months of follow up
Proportion who would avoid splenectomy at 6 months of follow up
Secondary Outcome Measures
SR,IR
Sustained response (platelet count that remained above 30X109/L or 2 folds of initial platelet count at 6 months of follow up) Initial response (an increase in the platelet count of at least 10X109/L or a platelet count of more than 30X109/L by day 7 after the initiation of treatment) Changes of platelet counts Safety of treatment Response rate of HP infected patients Decrement of steroid dose Predictors of response
Full Information
NCT ID
NCT01162941
First Posted
July 14, 2010
Last Updated
July 14, 2010
Sponsor
Cooperative Study Group A for Hematology
1. Study Identification
Unique Protocol Identification Number
NCT01162941
Brief Title
Efficacy of Helicobacter Pylori Eradication, Anti-D and Danazol Combination in Steroid Dependant or Refractory Immune Thrombocytopenia (ITP)
Official Title
Efficacy of Helicobacter Pylori Eradication, Anti-D and Danazol Combination in Steroid Dependant or Refractory Immune Thrombocytopenia (ITP)
Study Type
Interventional
2. Study Status
Record Verification Date
July 2010
Overall Recruitment Status
Unknown status
Study Start Date
February 2010 (undefined)
Primary Completion Date
July 2011 (Anticipated)
Study Completion Date
January 2012 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Cooperative Study Group A for Hematology
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Proportion who would avoid splenectomy at 6 months of follow up
Detailed Description
If urea breath test (+); omeprazole 20mg bid, amoxicillin 1000mg bid and clarithromycin 500mg bid for 1 week.
Second line Helicobacter pylori eradication will be permitted after failure of first line treatment.
Anti-D Anti-Ro 50 μg/kg IV for 2 days (D1, 2)
Danazol maintenance (from D1): Danazol will be continued at least 3 months. The dose of danazol can be reduced according to the adverse effects, especially in premenopausal women.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thrombocytopenia
Keywords
ITP
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
38 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Steroid dependant ITP
Arm Type
Experimental
Arm Description
more than 10 mg of prednisolone per day is required to maintain a platelet count above 20X109/L (minimum follow up duration: 3 months after diagnosis)
Intervention Type
Other
Intervention Name(s)
Steroid refractory ITP
Other Intervention Name(s)
prednisolone 1mg/kg
Intervention Description
a platelet count less than 20X109/L despite of treatment with full dose of steroid (prednisolone 1mg/kg for at least 4 weeks)
Primary Outcome Measure Information:
Title
Proportion who would avoid splenectomy at 6 months of follow up
Description
Proportion who would avoid splenectomy at 6 months of follow up
Time Frame
2years
Secondary Outcome Measure Information:
Title
SR,IR
Description
Sustained response (platelet count that remained above 30X109/L or 2 folds of initial platelet count at 6 months of follow up) Initial response (an increase in the platelet count of at least 10X109/L or a platelet count of more than 30X109/L by day 7 after the initiation of treatment) Changes of platelet counts Safety of treatment Response rate of HP infected patients Decrement of steroid dose Predictors of response
Time Frame
2years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1.ITP is defined by
(a) a true thrombocytopenia on blood smear, (b) adequate megakaryopoiesis on bone marrow examination, (c) the absence of clinically apparent associated conditions or cause of thrombocytopenia
2.Steroid dependant ITP: more than 10 mg of prednisolone per day is required to maintain a platelet count above 20X109/L (minimum follow up duration: 3 months after diagnosis)
3.Steroid refractory ITP: a platelet count less than 20X109/L despite of treatment with full dose of steroid (prednisolone 1mg/kg for at least 4 weeks)
4.18 years old or more
Exclusion Criteria:
1.Patients who have a cause of thrombocytopenia such as HIV infection, lymphoproliferative disease, liver disease, definite SLE or drug
2.Pregnancy
3.Splectomized patients
4.Rh- blood type
5.Hemoglobin < 10g/dL
6.Known hypersensitivity to immunoglobulins
7.A positive direct antiglobulin test
8.Clinically relevant hepatic or renal disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sung-Hwa Bae, professor
Phone
82-53-650-4388
Email
sunghwa@cu.ac.kr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jung-Hee Lee, professor
Organizational Affiliation
Asan Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Asan Medical Center
City
Seoul
State/Province
Asanbyeongwon-gil, songpa-gu
ZIP/Postal Code
138-736
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yae-Eun Jang, nurse
Phone
82-2-3010-6378
Email
redpin75@paran.com
12. IPD Sharing Statement
Links:
URL
http://www.google.co.kr
Description
Efficacy of Helicobacter pylori eradication, anti-D and danazol combination in steroid dependant or refractory immune thrombocytopenia (ITP)
Learn more about this trial
Efficacy of Helicobacter Pylori Eradication, Anti-D and Danazol Combination in Steroid Dependant or Refractory Immune Thrombocytopenia (ITP)
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