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Randomised Comparison of Cyclical Anthracycline-Based Chemotherapy [PA(BI)OE] with Alternating Chemotherapy [ChlVPP/PABIOE] in Advanced Hodgkin's Disease
Source of recordUK Trials
ISRCTNISRCTN46778796
Date ISRCTN assigned19/08/2002
Local reference number(s)LY2
Public titleRandomised Comparison of Cyclical Anthracycline-Based Chemotherapy [PA(BI)OE] with Alternating Chemotherapy [ChlVPP/PABIOE] in Advanced Hodgkin's Disease
Scientific title
AcronymNot Applicable
Disease/condition/study domainLymphoma (Hodgkin's)
Study hypothesisNot provided at time of registration
Design/methodologyRandomised controlled trial
Research ethics reviewNot provided at time of registration
Countries of trialUnited Kingdom
Participants - inclusion criteria1. All previously untreated and properly staged patients aged between 15 and 69 years (inclusive) with Hodgkin's disease for whom chemotherapy is indicated are eligible for this trial, ie Stage I & IIA (poor prognosis), IB, IIB, III, IV
2. Patients must be free from any irreversible medical condition that would drastically limit their life span or prohibit the use of combination chemotherapy. This applies particularly to elderly patients
3. Adequate long term follow-up must be possible
Participants - exclusion criteriaNot provided at time of registration
Patient information material
Anticipated end date30/04/1996
Status of trialCompleted
Target number of participantsNot provided at time of registration
Interventions1. PA(BI)OE Regimen: Multi-drug chemotherapy with adriamycin, vincristine, prednisolone, etoposide and bleomycin [PA(BI)OE] cycle repeated every 21 days. A minimum of six courses to be given with at least two following documentation of clinical complete remission and a maximum of eight courses. Bleomycin to be given for the first four courses only.

2. ChlVPP/PABIOE Regimen: Multi-drug chemotherapy with chlorambucil, procarbazine, prednisolone and vinblastine (ChIVPP) alternating every 21 days with PABIOE.
Primary outcome measure(s)Not provided at time of registration
Secondary outcome measure(s)Not provided at time of registration
Sources of fundingBritish National Lymphoma Investigation, Central Lymphoma Group
Sponsor nameBritish National Lymphoma Investigation (BNLI)
Sponsor detailsCRC and UCL Cancer Trials Centre
222 Euston Road
London
United Kingdom
NW1 2DA
Sponsor telephone+44(0)20 7679 8060
Sponsor fax+44(0)20 7679 8061
Sponsor emailbnli@ctc.ucl.ac.uk
Sponsor websitehttp://www.bnli.ucl.ac.uk
Contact nameDr - -
Contact detailsUKCCCR Register Co-ordinator
MRC Clinical Trials Unit
222 Euston Road
London
United Kingdom
NW1 2DA
Contact telephone+44 (0) 20 7670 4723
Contact fax+44 (0) 20 7670 4818
Contact emailregister@ctu.mrc.ac.uk
More informationFor more up-to-date information please go to the ISRCTN link below.
Link to record in ISRCTN RegisterISRCTN46778796
Date last extracted from ISRCTN register17/04/2008
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