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OpenTrials
Completed

NCT Number: NCT00598728

Quality of Life Among Survivors of Hodgkin Lymphoma

The purpose of this study is to collect information on the long-term side effects of treatment for Hodgkin Lymphoma. We hope to study about 500-800 survivors of Hodgkin Lymphoma. We plan to use the findings from this study to better understand Hodgkin Lymphoma survivors' health and quality of life.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Memorial Sloan-Kettering Cancer Center

New York, 10065, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Biopsy-proven HL Participation in IRB-approved protocols for the first-line treatment of HL between 1975-2000 (IRB #75-104, #75-103, #79-17, #81-103, #90-44, #91-69).
  • English speaking

Exclusion criteria

  • None

Treatment and study plan

Quality of Life Questionaires

Behavioral

A patient questionnaire, which includes questions on medical morbidities and QOL, will be mailed to participants.

Primary outcomes

  1. To evaluate the prevalence of late medical complications among HL survivors

    Time frame: conclusion of study

Secondary outcomes

  1. To study the effect of HL and its treatment on QOL among HL survivors.

    Time frame: conclusion of study

Sponsors and collaborators

Lead sponsor

Memorial Sloan Kettering Cancer Center

Other

Registry information

Official study title

A Global Assessment of Medical Morbidities and Quality of Life Among Survivors of Hodgkin Lymphoma

Important dates

Study start
2005
Primary completion
2016
Study completion
2016
First posted
Jan 22, 2008
Registry last updated
Apr 27, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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