HODGSA: Elderly Hodgkin Lymphoma Patients Treated With Chemoradiotherapy
Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Unknown status
CT.gov ID
NCT03535948
Collaborator
(none)
90
2
18.6
45
2.4
Study Details
Study Description
Brief Summary
Outcome of Hodgkin lymphoma patients over than 60 years treated by chemotherapy and/or radiotherapy: retrospective analysis.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
90 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Outcome of Hodgkin Lymphoma Patients Over Than 60 Years Treated by Chemotherapy and/or Radiotherapy: a Retrospective Study
Actual Study Start Date
:
May 15, 2018
Anticipated Primary Completion Date
:
Nov 30, 2019
Anticipated Study Completion Date
:
Dec 1, 2019
Outcome Measures
Primary Outcome Measures
- Progression-free survival [Time between diagnosis and progression or death - up to 100 weeks]
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months
Eligibility Criteria
Criteria
Ages Eligible for Study:
60 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
-
Patients over than 60 years
-
Newly diagnosed Hodgkin lymphoma
Exclusion Criteria:
- Data not available
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | CHU Dijon | Dijon | France | 21000 | |
2 | CHRU Nancy | Vandœuvre-lès-Nancy | France | 54500 |
Sponsors and Collaborators
- Central Hospital, Nancy, France
Investigators
- Principal Investigator: Lauriane Filliatre-Clement, CHRU Nancy
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT03535948
Other Study ID Numbers:
- PSS2016/hodgSA-CLEMENT-F/AS
First Posted:
May 24, 2018
Last Update Posted:
Jun 17, 2019
Last Verified:
May 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: