Hodgkin´s Lymphoma Clinical Trial
NCT number | NCT00264953 |
Other study ID # | HD11 |
Secondary ID | |
Status | Completed |
Phase | Phase 3 |
First received | December 12, 2005 |
Last updated | August 3, 2011 |
Start date | May 1998 |
This study is designed to (1) compare the efficacy of the BEACOPP regimen with that of ABVD as a 4-cycle chemotherapy combined with an involved field irradiation and (2) to define the optimum radiation dose comparing of 30 to 20 Gy in the same context.
Status | Completed |
Enrollment | 1395 |
Est. completion date | |
Est. primary completion date | January 2003 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 16 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Hodgkin´s lymphoma (histologically proven) - CS (PS) IA, IB, IIA, with one of the risk factors a-d CS (PS) IIB only with risk factor c or d 1. bulky mediastinal mass (> 1/3 maximum transverse thorax diameter) 2. extranodal involvement 3. ESR > 50 (A), > 30 (B-symptoms) 4. 3 or more lymph node areas involved - written informaed consent Exclusion Criteria: - Leukocytes <3000/microl - Platelets <100000/microl - Hodgkin´s Disease as "composite lymphoma" - Activity index (WHO) < grade 2 |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Cologne |
Eich HT, Diehl V, Görgen H, Pabst T, Markova J, Debus J, Ho A, Dörken B, Rank A, Grosu AL, Wiegel T, Karstens JH, Greil R, Willich N, Schmidberger H, Döhner H, Borchmann P, Müller-Hermelink HK, Müller RP, Engert A. Intensified chemotherapy and dose-reduce — View Citation
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