Trials / Unknown
UnknownNCT03010579
Erythropoietin in the Treatment of Anemia After Autologous Hematopoietic Stem Cell Transplantation
Efficacy and Safety of Erythropoietin in the Treatment of Anemia in Patients With Lymphoma After Autologous Hematopoietic Stem Cell Transplantation
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 70 (estimated)
- Sponsor
- Peking University · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
This is an randomized trial to evaluate the potential benefit of erythropoietin in the treatment of anemia in patients with lymphoma after autologous hematopoietic stem cell transplantation.
Detailed description
Lymphoma patients with anemia on day +15 post-transplant will be randomized to erythropoietin group or control group. Potential benefit of erythropoietin will be evaluatedon day +60 post-transplant.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | erythropoietin | Erythropoietin will be administered subcutaneously (s.c.) at the dose of 10 000 IU, three times a week. If necessary,oral ferrous succinate vitamins B12 and folic acid will be administered. |
| DRUG | iron supplementation | If necessary, oral ferrous succinate, vitamins B12 and folic acid will be administered. |
Timeline
- Start date
- 2016-10-01
- Primary completion
- 2017-12-01
- Completion
- 2018-12-01
- First posted
- 2017-01-05
- Last updated
- 2017-01-05
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT03010579. Inclusion in this directory is not an endorsement.