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CompletedNCT00186251Updated Nov 12, 2012

High Dose Chemotherapy Followed By PBSC Rescue for HD

An interventional study of high dose chemo then auto hematopoietic cell transplant in Hodgkin Disease, sponsored by Stanford University. Completed at 1 site in United States. Open to participants aged 4 Weeks to 70 Years. Per ClinicalTrials.gov, last updated 2012-11-12.

Sponsored by Stanford University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Non-randomized
Ages
4 Weeks to 70 Years
Sex
All
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Study summary

To evaluate the role of high dose chemotherapy with autologous hematopoietic cell transplantation in the treatment of Hodgkin's Disease.

Read the detailed description

Use of High Dose Chemotherapy Followed by Peripheral Blood Stem Cell Rescue for Relapsed or Resistant Hodgkin's Disease

02

Conditions studied

  • Hodgkin Disease

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03

In context

Hodgkin Disease

914 studies on the registry are indexed under Hodgkin Disease; 136 are open to participants now.

This study's enrollment of 200 is above the median of 43 across 746 interventional studies indexed under Hodgkin Disease.

Browse Hodgkin Disease studies →

Lead sponsor

Stanford University is the lead sponsor of 2,161 studies on the registry; 428 are open to participants now.

Of its 268 completed or terminated interventional studies of FDA-regulated products, 207 (77%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
4 Weeks to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:- adequate organ function

  • recurrent HD Exclusion Criteria:- CNS disease
  • no prior malignancy
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
200 participants

Interventions

  • Procedurehigh dose chemo then auto hematopoietic cell transplant
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What researchers measure

Primary outcomes

  1. Overall survival

  2. FFS

  3. Response rates

Secondary outcomes

  1. Toxicity of high dose chemotherapy

07

Study locations

1 site
  • Stanford University School of Medicine
    Stanford, California 94305, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 12, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00186251
First posted
Sep 16, 2005
Start date
Mar 1998
Completion
Jul 2005
Last update
Nov 12, 2012

Study contacts

Sally Arai
principal investigator · Stanford University
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2012. You cannot join it, but the record below documents what was studied.

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